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【结 构 式】

【分子编号】28918

【品名】3,4-diethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine

【CA登记号】

【 分 子 式 】C10H17N3

【 分 子 量 】179.2652

【元素组成】C 67% H 9.56% N 23.44%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(Vb)

The tetahydroimidazopyridine (I) is prepared by condensation of histamine with propionaldehyde in the presence of NaOH. The alkylation in position 1 or 3 is performed with ethyl bromide in a catalytic two-phase system, after protection of the amine group in position 5 as benzyloxycarbonyl derivative, and followed by removal of the protecting group by catalytic hydrogenation. The resulting amines (IVa-b) are then made to react with isopropyl isothiocyanate and the two regioisomers obtained are separated by crystallization.

1 Acari, G.; Bernardi, L.; Falconi, G.; Scarponi, U. (Pharmacia Corp.); 4,5,6,7-Tetrahydroimidazo[4,5-c]pyridine derivatives. BE 0871985; DE 2849572; FR 2433022; GB 2028798; JP 55024158; US 4223146 .
2 Riva, F.; 386/1634. Drugs Fut 1985, 10, 2, 101.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IVa) 28915 benzyl 1,4-diethyl-1,4,6,7-tetrahydro-5H-imidazo[4,5-c]pyridine-5-carboxylate C18H23N3O2 详情 详情
(IVb) 28916 benzyl 3,4-diethyl-3,4,6,7-tetrahydro-5H-imidazo[4,5-c]pyridine-5-carboxylate C18H23N3O2 详情 详情
(Va) 28917 1,4-diethyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine C10H17N3 详情 详情
(Vb) 28918 3,4-diethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine C10H17N3 详情 详情
(VIIa) 28920 1,4-diethyl-N-isopropyl-1,4,6,7-tetrahydro-5H-imidazo[4,5-c]pyridine-5-carbothioamide C14H24N4S 详情 详情
(VIIb) 28921 3,4-diethyl-N-isopropyl-3,4,6,7-tetrahydro-5H-imidazo[4,5-c]pyridine-5-carbothioamide C14H24N4S 详情 详情
(I) 28913 4-ethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine C8H13N3 详情 详情
(II) 10101 Benzyloxycarbonyl chloride; Benzyl chloroformate; 1-[[(Chlorocarbonyl)oxy]methyl]benzene 501-53-1 C8H7ClO2 详情 详情
(III) 28914 benzyl 4-ethyl-3,4,6,7-tetrahydro-5H-imidazo[4,5-c]pyridine-5-carboxylate C16H19N3O2 详情 详情
(VI) 28919 2-isothiocyanatopropane 2253-73-8 C4H7NS 详情 详情
Extended Information