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【结 构 式】

【分子编号】66024

【品名】 

【CA登记号】 

【 分 子 式 】C9H19NO.HCl

【 分 子 量 】193.717

【元素组成】C 55.80% H 10.41% N 7.23% O 8.26% Cl 18.30%

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:(XXXVIII)

Intermediates (III) and (XII) are prepared as follows:
Trimethyl orthooctanoate (XII) is prepared by Pinner reaction of octanonitrile (XXXVII) with MeOH in the presence of HCl in MeOAc followed by treatment of the resulting methyl octanimidate hydrochloride (XXXVIII) with MeOH in methylcyclohexane (3). Scheme 5.
Intermediate (III) can be prepared by consecutive N-protection of the amidine nitrogens in pyrazole-1-carboxamidine (XIV), first by treatment with Boc2O by means of DIEA in DMF, and then reaction of the resulting monoprotected intermediate (XXXIX) with Boc2O in the presence of NaH in THF (3). Scheme 5.

3 Nakamura, Y., Murakami, M., Yamaoka, M., Wakayama, M., Umeo, K. (Daiichi Sankyo Co., Ltd.). Method for manufacturing neuraminic acid derivatives. EP 2132191, JP 2010523472, WO 2008126943.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(III) 52079 sodium (Z)-1-cyano-3-ethoxy-3-oxo-1-propen-2-olate 627076-29-3 C6H6NNaO3 详情 详情
(XII) 66000 trimethyl orthooctanoate; 1,1,1-Trimethoxyoctane 161838-87-5 C11H24O3 详情 详情
(XIV) 15983 1H-pyrazole-1-carboximidamide 4023-00-1 C4H6N4 详情 详情
(XXXVII) 59081 octanenitrile 124-12-9 C8H15N 详情 详情
(XXXVIII) 66024     C9H19NO.HCl 详情 详情
(XXXIX) 66025 N-(tert-Butoxycarbonyl)-1H-pyrazole-1-carboxamidine; N-Boc-1H-pyrazole-1-carboxamidine 152120-61-1 C9H14N4O2 详情 详情
Extended Information