CAS Registry Number: 107783-37-9
Taxonomy: Physicochemical and Pharmacological Properties of Alkaloids – Quinoline Alkaloids
Biological sources: Haplophyllum obtusifolium
C18H18NO4Cl: 349.0895/347.0924
Mp: 151–153°C (Me2CO) [1]
UV: 251, 319, 330 (4.73, 3.60, 3.67) [1]
IR: 3145, 3115, 1628, 1588, 1518, 1495, 1460, 1390, 1370, 1323, 1270, 1235, 1150, 1100, 1089, 1060, 1000, 990 [2]
MS m/z: 349(6.2), 347(M+, 19), 312(4), 245(50), 244(100), 230(10), 227(43), 216(31), 199(9) [1]
1 H NMR: 1.87(3H, s, CH3), 4.05(3H, s, OCH3), 4.09(2H, s, CH2Cl), 4.35(3H, s, OCH3), 4.78, 5.68(2H, d, 1H, t, J = 7, CH–CH2–O), 6.99, 7.53(each 1H, d, J = 2.8, H-3, H-2), 7.15, 7.93(each 1H, d, J = 9.4, H-6, H-5) [1]
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References
I.A. Bessonova, S.Yu. Yunusov, Chem. Nat. Comp. 22, 684 (1986)
R. Shakirov, M.V. Telezhenetskaya, I.A. Bessonova, S.F. Aripova, I.A. Israilov, M.N. Sultankhodzhaev, V.I. Vinogradova, V.I. Akhmedzhanova, T.S. Tulyaganov, B.T. Salimov, V.A. Tel’nov, Chem. Nat. Comp. 32, 932 (1996)
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(2013). Haplobine. In: Azimova, S.S., Yunusov, M.S. (eds) Natural Compounds. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0560-3_1153
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