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Ammonium Hydroxide → 1-[[2-(Phenylmethoxy)acetyl]amino]-1H-imidazole-5-carboxamide

HRID 57721
노트
인쇄 미리보기

반응식

HRID 57721 반응식
C[O:2][C:3]([C:5]1[N:6]([NH:10][C:11](=[O:21])[CH2:12][O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:7]=[N:8][CH:9]=1)=O.[OH-].[NH4+:23]>>[CH2:14]([O:13][CH2:12][C:11]([NH:10][N:6]1[C:5]([C:3]([NH2:23])=[O:2])=[CH:9][N:8]=[CH:7]1)=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 14923Ammonium HydroxideHCID 897151963-(2-Benzyloxy-acetylamino)-3H-imidazole-4-carboxylic acid methyl ester

생성물 1

HCID 897148121-[[2-(Phenylmethoxy)acetyl]amino]-1H-imidazole-5-carboxamide수율 88%

반응 조건

온도
70 °C

실험 절차

Compound 2 (8.7 g, 30.1 mmol) and ammonium hydroxide (15 ml) were combined in a sealed tube and heated to 70° C. under microwave irradiation for 2 hours. The mixture was concentrated in vacuo to afford compound 3 (7.3 g, 88% yield) as a white solid. LC-MS: m/z 275.1 [M+H]+.

후처리

  1. concentrationThe mixture was concentrated in vacuo

출처 및 근거

ORD 기록
ord-c9d80954d63d4e63b59351e0de4a8653
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434733B2

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