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Hydrochloric Acid → 1-(3-aminopropyl)-2-(methoxycarbonyl)-1H-benzimidazole-6-carboxylic acid hydrochloride

HRID 1521687
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인쇄 미리보기

반응식

HRID 1521687 반응식
C(OC([NH:8][CH2:9][CH2:10][CH2:11][N:12]1[C:16]2[CH:17]=[C:18]([C:21]([OH:23])=[O:22])[CH:19]=[CH:20][C:15]=2[N:14]=[C:13]1[C:24](OC)([O:27]C)[O:25][CH3:26])=O)(C)(C)C.[ClH:31]>CO>[ClH:31].[NH2:8][CH2:9][CH2:10][CH2:11][N:12]1[C:16]2[CH:17]=[C:18]([C:21]([OH:23])=[O:22])[CH:19]=[CH:20][C:15]=2[N:14]=[C:13]1[C:24]([O:25][CH3:26])=[O:27]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 672353441-{3-[(tert-Butoxycarbonyl)amino]propyl}-2-(trimethoxymethyl)-1H-benzimidazole-6-carboxylic acid2회

생성물 1

HCID 672365501-(3-aminopropyl)-2-(methoxycarbonyl)-1H-benzimidazole-6-carboxylic acid hydrochloride수율 92%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 1-{3-[(tert-Butoxycarbonyl)amino]propyl}-2-(trimethoxymethyl)-1H-benzimidazole-6-carboxylic acid (Intermediate A, 20 g, 68.7 mmol) in methanol (200 mL) is added conc. HCl (5 mL) and the reaction mixture is stirred at room temperature for 1 h. The solvent is evaporated to afford the title compound as a solid (20 g, 92%) which is used in the next reaction without purification.

후처리

  1. customThe solvent is evaporated

출처 및 근거

ORD 기록
ord-6cb53b1d9b8f4e2e859b91a782b66ac0
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073926B2

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