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【结 构 式】

【分子编号】33779

【品名】(10R)-10-hydroxy-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide

【CA登记号】

【 分 子 式 】C15H14N2O2

【 分 子 量 】254.28844

【元素组成】C 70.85% H 5.55% N 11.02% O 12.58%

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:(IIb),(VI)

Oxcarbazepine (I) was reduced with NaBH4 to afford the racemic alcohol (IIa-b). Esterification with (-)-menthoxyacetic acid chloride (III) in the presence of dimethylaminopyridine provided the diastereomeric mixture of esters (IV) and (V), from which the desired isomer (V) was isolated by fractional crystallization from CH2Cl2/EtOAc. Basic hydrolysis of (V) then provided pure (R)-alcohol (VI). Finally, esterification of (VI) with acetyl chloride led to the title acetate ester.

1 Garrett, J.; Soares-da-Silva, P.; Freitas, A.P.; Cunha, R.A.; Benes, J.; Parada, A.; Learmonth, D.A.; Alves, P.C.; Figueiredo, A.; Anticonvulsant and sodium channel-blocking properties of novel 10,11-dihydro-5H-dibenz[b,f]azepine-5-carboxamide derivatives. J Med Chem 1999, 42, 14, 2582.
2 Benes, J.; Vieira Araujo Soares da Silva, P.M. (Portela & Ca., SA); Substd. dihydrodibenzo[b,f]azepines, method of their preparation, their use in the treatment of some central nervous system disorders, and pharmaceutical compsns. containing them. EP 0751129; US 5753646 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IIa) 33775 (10S)-10-hydroxy-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide C15H14N2O2 详情 详情
(IIb),(VI) 33779 (10R)-10-hydroxy-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide C15H14N2O2 详情 详情
(I) 33774 10-oxo-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide 28721-07-5 C15H12N2O2 详情 详情
(III) 33776 2-[[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy]acetyl chloride 15356-62-4 C12H21ClO2 详情 详情
(IV) 33777 (10S)-5-(aminocarbonyl)-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl 2-[[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy]acetate C27H34N2O4 详情 详情
(V) 33778 (10R)-5-(aminocarbonyl)-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl 2-[[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy]acetate C27H34N2O4 详情 详情
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