Introduction

Studies on steroids stimulated renewed interest because apart from their estrogenic and anabolic/androgenic activity [1–3] steroids were found to show various biological activities including cytotoxicity [4], antiproliferative activity [5], antimicrobial activity [6], anti-glioma activity [7], inhibition of cholesterol α-glucosyltransferase [8], neuromuscular blocking activity [9], differential activities on prostate cancer cells [10], anti-osteoporosis activity [11], and anti-aging activity [12]. Up until now steroids have showed potential applications as 5α-reductase inhibitors [13], as modulators of inflammation and immunity [14], as inhibitors of 17α-hydroxylase/C17,20-lyase [15], as predictor of tamoxifen response in premenopausal breast cancer [16], as progesterone receptor antagonist [17], as glucocorticoid receptor imaging agents [18], as inhibitors of protein tyrosine phosphatase 1B [19], as reversal agents of multidrug resistance in cancer cells [20], as inhibitors of 17β-hydroxysteroid dehydrogenase [21], and as ligands for drug vectors [22]. Some steroidal compounds were used for photodynamic therapy [23], for cancer chemotherapy [24], and for DNA delivery [25]. Moreover, cholesteric liquid crystal [26] and steroid-based organogelator [27] were also studied. Recently Cabeza and collegues synthesized a series of 3β-benzoyloxy-4,16-pregnadiene-6,20-dione (1a-e, Figure 1) and 3β- cycloalkylcarbonyloxy-4,16-pregnadiene-6,20-dione (2a-d, Figure 1) compounds starting from 16-dehydropregnenolone acetate (16-DPA) and evaluated their biological activities. Of these steroids 1a is a good inhibitor for the 5α-reductase enzyme [13] while 1b-e and 2a-d showed high antiandrogenic activity [28, 29]. In continuation of our study on steroids [30, 31] and to explore an improved way for synthesis of new steroidal compounds from the cheap starting material diosgenin, herein we report the synthesis and structural characterization of a series of new aromatic esters based on 4,16-pregnadiene-6,20-dione skeleton.

Figure 1
figure 1

Chemical structure of compound 1a-e and 2a-d.

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Experimental

All chemical reagents were purchased from commercial sources and used as received unless stated otherwise. Melting points were determined on a XT-4 melting apparatus and the quoted temperatures were uncorrected. Elemental analysis was carried out on an Elmentar Vario EL III system. 1H NMR and 13C NMR spectra were recorded on a Bruker AM 400 spectrometer. CDCl3 was used as solvent and chemical shifts recorded were internally referenced to Me4Si (0 ppm). IR spectra were obtained on a Thermo Electron Corporation Nicolet 380 FT-IR spectrophotometer. Mass spectra were recorded on a Shimadzu QP-2010 instrument using electron impact ionization (EI) at 70 eV. LC-MS spectra were obtained on an Agilent 6000 LC-MS instrument equipped with a SunFire C18 column (4.6 × 50 mm, 3.5 μm) under the following conditions: mobile phase: H2O (0.05% trifluoroacetic acid (TFA)) (A)/acetonitrile (0.05% TFA) (B); elution program: gradient from 5 to 95% of B in 1.6 min at 2.2 ml/min; temperature: 50°; detection: UV (214 nm) and MS (ESI, pos mode, 70 to 1000 amu). All of the measured samples were dissolved in methanol. X-Ray crystal structure was measured on a Bruker Smart CCD diffractometer by using Mo Kα radiation at 293 K.

Pseudodiosgenin diacetate (4) [32]

To a solution of diosgenin 3 (16.0 g, 38.6 mmol) and ammonium chloride (2.5 g, 46.7 mmol) in acetic anhydride (82 ml) was added pyridine (1.5 ml) and the mixture was heated at 140°C for 8-9 h. The resulting solution was cooled to room temperature and poured into ice water. The precipitate was filtered and recrystallized from methanol to give the product pseudodiosgenin diacetate (4) as yellow solid (16.6 g, 86%). M.p. 70-72°C.

3β-Acetoxy-5,16-pregnadiene-20-one (5)

A solution of pseudodiosgenin diacetate (4) (15.4 g, 30.8 mmol) in acetic anhydride (76 ml) was diluted with water (4.8 ml) and acetic acid (50 ml). The mixture was cooled to 0°C then a solution of chromium(VI) oxide (8.9 g, 89.0 mmol) in acetic acid (25 ml) was added dropwise in 1 h. After the addition the solution was allowed to warm to 10-16°C and the stirring was continued for 5 h at this temperature. Sodium bisulphite (9.3 g, 89.4 mmol) in water (30 ml) was added then the mixture was refluxed for 3 h, cooled and poured into water to give sticky solids. The crude product was crystallized from methanol then purified by means of column chromatography on silica gel with petroleum ether (b.p. 60-90°C) and ethyl acetate (4:1, v/v) as eluent to afford product 5 (4.5 g, 41%) as yellow needles. M.p. 170-172°C (literature [32] value: 171-172°C). Rf 0.58 (petroleum ether/ethyl acetate, 4:1, v/v).

Compound 6 was synthesized as described in literature [33] in 90% yield and as described in literature [13] in 95% yield. M.p. 170-172°C (literature [13] value: 170-172°C). Rf 0.57 (petroleum ether/ethyl acetate, 4:1, v/v).

Compound 7 was synthesized as described in literature [13] in 84% yield. M.p. 243-245°C (literature [13] value: 244-245°C). Rf 0.56 (petroleum ether/ethyl acetate, 4:1, v/v).

Compound 8 was synthesized as described in literature [13] in 73% yield. M.p. 192-194°C (literature [13] value: 193-195°C). Rf 0.58 (petroleum ether/ethyl acetate, 4:1, v/v).

3β-Hydroxypregna-4,16-diene-6,20-dione (9)

A solution of steroid 8 (0.3 g, 0.8 mmol) in methanol (45 ml) and 2% aqueous sodium hydroxide (3 ml) was stirred for 30 min at room temperature. The resulting solution was poured into ice water (45 ml) then extracted with ethyl acetate (3 × 30 ml). The organic phase was dried over anhydrous magnesium sulfate and the solvent was removed in vacuum. The residue was purified by column chromatography on silica gel with petroleum ether and ethyl acetate (1:1, v/v) as eluent to afford product 9 (0.25 g, 74%) as pale yellow needles. M.p. 168-170°C (literature [13] value: 168-170°C). Rf 0.52 (petroleum ether/ethyl acetate, 4:1, v/v).

3β-(p-Methoxybenzoyloxy)pregna-4,16-diene-6,20-dione (10a)

A solution containing steroid 9 (0.10 g, 0.3 mmol), p-methoxybenzoic acid (0.13 g, 0.7 mmol), 1,3-dicyclohexylcarbodiimide (DCC, 0.10 g, 0.5 mmol) and 4-dimethylaminopyridine (DMAP, 0.06 g, 0.5 mmol) in methylene dichloride (6 ml) was stirred for 2 h at about 10°C. Ice water was added and the reaction mixture was extracted with chloroform (3 × 20 ml). The organic phase was dried over anhydrous magnesium sulfate and the solvent was removed in vacuum. The crude product was dissolved in ethyl acetate and filtered through a column containing silica gel. The organic solvent was removed in vacuum to give a white crystalline solid 10a (0.14 g, 71%). M.p. 244-246°C. Rf 0.50 (petroleum ether/ethyl acetate, 4:1, v/v). 1H NMR (CDCl3): 0.94 (s, 3 H, H-C(18)); 1.10 (s, 3 H, H-C(19)); 2.28 (s, 3 H, H-C(21)); 3.87 (s, 3 H, OMe); 5.56 (m, 1 H, H-C(3)); 6.23 (m, 1 H, H-C(4)); 6.71 (t, 1 H, J = 1.3 Hz, H-C(16)); 6.93 (m, 2 H, H-Ph); 8.02 (m, 2 H, H-Ph). 13C NMR (CDCl3): 15.8 (C(18)); 19.7 (C(19)); 27.1 (C(21)); 69.5 (C(3)); 131.8 (C(4)); 143.8 (C(16)); 147.9 (C(5)); 154.9 (C(17)); 165.9 (ester C = O); 196.6 (C(20)); 201.9 (C(6)). IR (KBr): 3075, 2958, 1706, 1690, 1656, 1629. EI-MS: 312 (12, M+ + 1 - p-MeO-C6H4COO), 175 (31), 157 (38), 121 (30), 105 (41), 93 (33), 91 (66), 79 (51), 77 (46), 43 (100). LC-MS: 485.4 (M+ + Na, retention time 2.20 min). Anal. Calcd. for C29H34O5: C, 75.30; H, 7.41; Found: C, 75.12; H, 7.37.

Other steroidal compounds 10b-j were prepared in a similar procedure and the physical data of the new steroids were as follows.

3β-(o-Methoxybenzoyloxy)pregna-4,16-diene-6,20-dione (10b)

White powder. Yield 45%. M.p. 240-242°C. Rf 0.42 (petroleum ether/ethyl acetate, 4:1, v/v). 1H NMR (CDCl3): 0.93 (s, 3 H, H-C(18)); 1.07 (s, 3 H, H-C(19)); 2.27 (s, 3 H, H-C(21)); 3.89 (s, 3 H, OMe); 5.56 (m, 1 H, H-C(3)); 6.23 (m, 1 H, H-C(4)); 6.73 (t, J = 1.6 Hz, H-C(16)); 6.96 (m, 2 H, H-Ph); 7.46 (m, 1 H, H-Ph); 7.80 (m, 1 H, H-Ph). 13C NMR (CDCl3): 17.5 (C(18)); 22.0 (C(19)); 26.5 (C(21)); 71.8 (C(3)); 136.0 (C(4) and C(16)); 146.1 (C(5)); 149.9 (C(17)); 167.0 (ester C = O); 198.9 (C(20)); 203.8 (C(6)). IR (KBr): 3040, 2946, 1688. LC-MS: 485.4 (M+ + Na, retention time 2.13 min). Anal. Calcd. for C29H34O5: C, 75.30; H, 7.41; Found: C, 75.04; H, 7.46.

3β-(o-Methylbenzoyloxy)pregna-4,16-diene-6,20-dione (10c)

White powder. Yield 62%. M.p. 182-184°C. Rf 0.39 (petroleum ether/ethyl acetate, 3:1, v/v). 1H NMR (CDCl3): 0.94 (s, 3 H, H-C(18)); 1.08 (s, 3 H, H-C(19)); 2.28 (s, 3 H, H-C(21)); 2.60 (s, 3 H, Me-Ph); 5.56 (m, 1 H, H-C(3)); 6.24 (m, 1 H, H-C(4)); 6.72 (t, 1 H, J = 1.8 Hz, H-C(16)); 7.23 (m, 2 H, H-Ph); 7.40 (m, 1 H, H-Ph); 7.93 (m, 1 H, H-Ph). 13C NMR (CDCl3): 15.8 (C(18)); 19.7 (C(19)); 27.1 (C(21)); 69.6 (C(3)); 132.1 (C(4)); 143.9 (C(16)); 148.0 (C(5)); 154.9 (C(17)); 168.4 (ester C = O); 196.7 (C(20)); 201.8 (C(6)). IR (KBr): 3070, 2946, 1688. LC-MS: 469.4 (M+ + Na, retention time 2.28 min). Anal. Calcd. for C29H34O4: C, 78.00; H, 7.67; Found: C, 77.81; H, 7.63.

3β-(m-Methylbenzoyloxy)pregna-4,16-diene-6,20-dione (10d)

White powder. Yield 69%. M.p. 138-140°C. Rf 0.42 (petroleum ether/ethyl acetate, 3:1, v/v). 1H NMR (CDCl3): 0.95 (s, 3 H, H-C(18)); 1.11 (s, 3 H, H-C(19)); 2.27 (s, 3 H, H-C(21)); 5.60 (m, 1 H, H-C(3)); 6.24 (m, 1 H, H-C(4)); 6.71 (t, 1 H, J = 1.8 Hz, H-C(16)); 7.32 (m, 2 H, H-Ph); 7.44 (m, 1 H, H-Ph); 7.84 (m, 1 H, H-Ph). 13C NMR (CDCl3): 15.8 (C(18)); 19.7 (C(19)); 27.1 (C(21)); 69.8 (C(3)); 138.0 (C(4)); 143.9 (C(16)); 148.0 (C(5)); 154.9 (C(17)); 166.4 (ester C = O); 196.6 (C(20)); 201.9 (C(6)). IR (KBr): 3060, 2945, 1688, 1589, 1457. LC-MS: 469.4 (M+ + Na, retention time 2.29 min). Anal. Calcd. for C29H34O4: C, 78.00; H, 7.67; Found: C, 78.18; H, 7.71.

3β-(p-Nitrobenzoyloxy)pregna-4,16-diene-6,20-dione (10e)

Pale yellow powder. Yield 46%. M.p. 174-176°C. Rf 0.36 (petroleum ether/ethyl acetate, 3:1, v/v). 1H NMR (CDCl3): 0.95 (s, 3 H, H-C(18)); 1.12 (s, 3 H, H-C(19)); 2.28 (s, 3 H, H-C(21)); 5.62 (m, 1 H, H-C(3)); 6.21 (m, 1 H, H-C(4)); 6.72 (t, 1 H, J = 1.8 Hz, H-C(16)); 8.23 (m, 2 H, H-Ph); 8.28 (m, 2 H, H-Ph). 13C NMR (CDCl3): 15.8 (C(18)); 19.6 (C(19)); 27.1 (C(21)); 71.0 (C(3)); 130.8 (C(4)); 135.4 (C(16)); 148.6 (C(5)); 154.9 (C(17)); 164.3 (ester C = O); 196.6 (C(20)); 201.8 (C(6)). IR (KBr): 3062, 2946, 1688, 1528, 1456. LC-MS: 500.3 (M+ + Na, retention time 2.17 min). Anal. Calcd. for C28H31NO6: C, 70.42; H, 6.54; N, 2.93; Found: C, 70.57; H, 6.52; N, 2.87.

3β-(o-Nitrobenzoyloxy)pregna-4,16-diene-6,20-dione (10f)

Pale yellow powder. Yield 55%. M.p. 158-161°C. Rf 0.29 (petroleum ether/ethyl acetate, 3:1, v/v). 1H NMR (CDCl3): 0.92 (s, 3 H, H-C(18)); 1.05 (s, 3 H, H-C(19)); 2.27 (s, 3 H, H-C(21)); 5.60 (m, 1 H, H-C(3)); 6.17 (m, 1 H, H-C(4)); 6.70 (t, 1 H, J = 1.8 Hz, H-C(16)); 7.63-7.68 (m, 2 H, H-Ph); 7.72 (m, 1 H, H-Ph); 7.95 (m, 1 H, H-Ph). 13C NMR (CDCl3): 15.8 (C(18)); 19.6 (C(19)); 27.1 (C(21)); 71.5 (C(3)); 133.0 (C(4)); 143.8 (C(16)); 148.6 (C(5)); 154.9 (C(17)); 165.1 (ester C = O); 196.6 (C(20)); 201.6 (C(6)). IR (KBr): 3033, 2945, 1732, 1687, 1656, 1628, 1587, 1540, 1456. LC-MS: 500.3 (M+ + Na, retention time 2.11 min). Anal. Calcd. for C28H31NO6: C, 70.42; H, 6.54; N, 2.93; Found: C, 70.25; H, 6.49; N, 2.90.

3β-(m-Nitrobenzoyloxy)pregna-4,16-diene-6,20-dione (10g)

Pale yellow powder. Yield 47%. M.p. 176-178°C. Rf 0.38 (petroleum ether/ethyl acetate, 3:1, v/v). 1H NMR (CDCl3): 0.94 (s, 3 H, H-C(18)); 1.12 (s, 3 H, H-C(19)); 2.27 (s, 3 H, H-C(21)); 5.63 (m, 1 H, H-C(3)); 6.20 (m, 1 H, H-C(4)); 6.71 (t, J = 1.2 Hz, H-C(16)); 7.66 (m, 1 H, H-Ph); 8.36-8.43 (m, 2 H, H-Ph); 8.86 (m, 1 H, H-Ph). 13C NMR (CDCl3): 15.8 (C(18)); 19.6 (C(19)); 27.1 (C(21)); 71.0 (C(3)); 135.4 (C(4)); 143.8 (C(16)); 148.6 (C(5)); 154.9 (C(17)); 164.1 (ester C = O); 196.6 (C(20)); 201.7 (C(6)). IR (KBr): 3040, 2945, 1689, 1526, 1456. LC-MS: 500.3 (M+ + Na, retention time 2.17 min). Anal. Calcd. for C28H31NO6: C, 70.42; H, 6.54; N, 2.93; Found: C, 70.27; H, 6.58; N, 2.88.

3β-(3,5-Dinitrobenzoyloxy)pregna-4,16-diene-6,20-dione (10h)

Pale yellow powder. Yield 45%. M.p. 168-170°C. Rf 0.59 (petroleum ether/ethyl acetate, 2:1, v/v). 1H NMR (CDCl3): 0.95 (s, 3 H, H-C(18)); 1.15 (s, 3 H, H-C(19)); 2.29 (s, 3 H, H-C(21)); 5.70 (m, 1 H, H-C(3)); 6.20 (m, 1 H, H-C(4)); 6.72 (t, 1 H, J = 1.4 Hz, H-C(16)); 9.16 (m, 2 H, H-Ph); 9.24 (m, 1 H, H-Ph). 13C NMR (CDCl3): 15.8 (C(18)); 19.5 (C(19)); 27.1 (C(21)); 72.2 (C(3)); 133.8 (C(4)); 143.8 (C(16)); 148.6 (C(5)); 154.8 (C(17)); 162.2 (ester C = O); 196.6 (C(20)); 201.6 (C(6)). IR (KBr): 3037, 2946, 1689, 1543, 1457. LC-MS: 500.3 (M+ + Na, retention time 3.14 min). Anal. Calcd. for C28H30N2O8: C, 64.36; H, 5.79; N, 5.36; Found: C, 64.22; H, 5.75; N, 5.19.

3β-(o-Chlorobenzoyloxy)pregna-4,16-diene-6,20-dione (10i)

White powder. Yield 64%. M.p. 192-194°C. Rf 0.32 (petroleum ether/ethyl acetate, 3:1, v/v). 1H NMR (CDCl3): 0.95 (s, 3 H, H-C(18)); 1.11 (s, 3 H, H-C(19)); 2.27 (s, 3 H, H-C(21)); 5.59 (m, 1 H, H-C(3)); 6.24 (m, 1 H, H-C(4)); 6.71 (t, 1 H, J = 1.8 Hz, H-C(16)); 7.32 (m, 1 H, H-Ph); 7.36 (m, 2 H, H-Ph); 7.87 (m, 1 H, H-Ph). 13C NMR (CDCl3): 15.8 (C(18)); 19.6 (C(19)); 27.1 (C(21)); 70.5 (C(3)); 133.9 (C(4)); 143.8 (C(16)); 148.2 (C(5)); 154.9 (C(17)); 165.2 (ester C = O); 196.6 (C(20)); 201.7 (C(6)). IR (KBr): 3040, 2946, 1688, 1522, 1456. LC-MS: 490.2 (M+ + Na, retention time 2.23 min). Anal. Calcd. for C28H31ClO4: C, 72.01; H, 6.69; Found: C, 71.83; H, 6.65.

3β-(2-Furoyloxy)pregna-4,16-diene-6,20-dione (10j)

White powder. Yield 77%. M.p. 180-182°C. Rf 0.40 (petroleum ether/ethyl acetate, 2:1, v/v). 1H NMR (CDCl3): 0.94 (s, 3 H, H-C(18)); 1.09 (s, 3 H, H-C(19)); 2.28 (s, 3 H, H-C(21)); 5.57 (m, 1 H, H-C(3)); 6.20 (m, 1 H, H-C(4)); 6.52 (t, 1 H, J = 1.8 Hz, H-C(16)); 6.71 (m, 1 H, H-Ar); 7.20 (m, 1 H, H-Ar); 7.59 (m, 1 H, H-Ar). 13C NMR (CDCl3): 15.8 (C(18)); 19.6 (C(19)); 27.1 (C(21)); 69.9 (C(3)); 128.7 (C(4)); 143.8 (C(16)); 148.1 (C(5)); 154.8 (C(17)); 158.3 (ester C = O); 196.6 (C(20)); 201.8 (C(6)). IR (KBr): 3042, 2946, 1720, 1689, 1657, 1580, 1523, 1457. LC-MS: 445.2 (M+ + Na, retention time 2.06 min). Anal. Calcd. for C26H30O5: C, 73.91; H, 7.16; Found: C, 73.73; H, 7.21.

Results and Discussion

The synthetic route of the target steroids 3β-benzoyloxypregna-4,16-diene-6,20-dione (10a-i) and 3β-furoyloxypregna-4,16-diene-6,20-dione (10j) was showed in Figure 2. At first the starting material diosgenin was transformed by acetylation and oxidation to 3β-acetoxy-5,16-pregnadiene-20-one (16-DPA, 5). The transformation could be achieved stepwise or in a one-pot reaction [32]. We adopted the former in consideration that the purification of the product was easier to yield 16-DPA of higher purity. Epoxidation of 16-DPA to form steroid 6 was conducted by using 30% H2O2/HCO2H [33] or m-chloroperoxybenzoic acid (m-CPBA) [13] oxidation system in 90% or 95% yield.

Figure 2
figure 2

Synthetic route of target steroids 10a-j.

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Conversion of compound 6 to 7 was carried out in a similar way as reported in literature [13] and the yield of steroid 7 was improved from 81% to 84%. Dehydration of 7 with thionyl chloride in pyridine resulted compound 8. We found that the quality of the solvent pyridine had an effect on the yield of the steroid 8. When dried pyridine (refluxed in the presence of potassium hydroxide for 2 h before distillation) was used instead of pyridine of analytically pure grade without treatment, the yield of 8 was improved to 73% from the literature [13] value 66%. Compound 8 was hydrolyzed with aqueous sodium hydroxide in methanol to afford 3β-hydroxypregna-4,16-diene-6,20-dione (9). The procedure for workup was improved by using extraction (with ethyl acetate) and concentration replacing filtration and subsequent recrystallization and pure product 9 was obtained in 74% yield, significantly higher than the literature [13] value 60%.

The target steroids 3β-benzoyloxypregna-4,16-diene-6,20-dione (10a-i) and 3β- furoyloxypregna-4,16-diene-6,20-dione (10j) were synthesized through Steglich reaction from 9, substituted benzoic acid or furoic acid, and DCC catalyzed by DMAP in fair to good yields (45%-77%), depending upon the structure of the aryl acids. It seems that the steric hindrance from the aryl acid structure leads to decrease in the yield. Therefore the highest yield of the Steglich reaction came from furoic acid (77%) while the reactions with dinitrobenzoic acid or nitrobenzoic acid gave the lowest yield.

The chemical structures of steroids 10a-j were fully characterized by elemental analysis, 1H NMR, 13C NMR, IR and mass spectrum and melting point measurements. Characteristic chemical shifts in 1H NMR spectra of steroids 10a-j were summarized in Table 1. All the chemical shifts of protons in methyl groups, OCH moieties, C = CH moieties, and aryl rings were in the reasonable range and the spectra data were in good accordance with the structures.

Table 1 Characteristic chemical shifts in 1H NMR spectra of steroids 10a-j
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Single crystals of 10a suitable for X-ray crystal diffraction measurement were obtained by slow evaporation of a solution of 10a in 1:1 petroleum ether and ethyl acetate. X-Ray data for crystals of 10a were collected by graphite-monochromatized Mo Kα radiation at 293 K and the crystal data and experimental details for compound 10a were summarized in Table 2. The structure was solved by direct methods and refined by full-matrix least-squares with anisotropic temperature factors for the non-hydrogen atoms. The hydrogen atoms bonded to the carbon atoms were assigned based on the expected bonding geometry. The hydrogen atoms were refined isotropically in the final least-squares cycles.

Table 2 Crystal data and experimental details for compound 10a
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The crystal structure and molecular packing of steroid 10a were shown in Figure 3 and Figure 4 respectively. It can be seen that the molecule consists of three six-membered rings (A, B, and C ring) and one five-membered ring (D ring), all trans fused. The six-membered rings A, B, and C occur in a half chair, distorted chair, and distorted chair conformation, respectively. Ring D adopts a distorted envelope conformation. The molecules in the crystal were packed face-to-face at the normal van der Waals distances, similar to the crystal structure of 3β-(p-fluorobenzoyloxy)-4,16-pregnadiene-6,20-dione [34]. CCDC-787721 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/data_request/cif

Figure 3
figure 3

Crystal structure of compound 10a.

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Figure 4
figure 4

View of the molecular packing in 10a.

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Conclusions

In summary, ten new aromatic esters based on 4,16-pregnadiene-6,20-dione skeleton, namely 3β-benzoyloxy-4,16-pregnadiene-6,20-dione and 3β-furoyloxy-4,16-pregnadiene-6,20- dione were synthesized starting from diosgenin. The structures of the steroids were characterized by elemental analysis, 1H NMR, 13C NMR, IR and mass spectrum. Single crystal X-ray diffraction measurement on one of the new compounds, 3β-(p-methoxybenzoyloxy)-4,16-pregnadiene-6,20-dione revealed that the A, B, C, and D ring adopted half chair, distorted chair, distorted chair, and distorted envelope conformation, respectively. The molecules in the crystal were packed face-to-face at the normal van der Waals distances. These new steroids may show high antiandrogenic activity and serve as good inhibitors for the 5α-reductase enzyme. Investigation of the inhibitory activity of the new steroids for the 5α-reductase enzyme will be conducted in the near future.