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Diisopropylethylamine → 1-(2-Fluoro-4-methanesulfonylphenyl)-1H-imidazole-4-carboxylic acid

HRID 1409731
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인쇄 미리보기

반응식

HRID 1409731 반응식
[NH:1]1[CH:5]=[C:4]([C:6]([OH:8])=[O:7])[N:3]=[CH:2]1.F[C:10]1[CH:15]=[CH:14][C:13]([S:16]([CH3:19])(=[O:18])=[O:17])=[CH:12][C:11]=1[F:20].C(N(CC)C(C)C)(C)C>CN(C)C=O>[F:20][C:11]1[CH:12]=[C:13]([S:16]([CH3:19])(=[O:18])=[O:17])[CH:14]=[CH:15][C:10]=1[N:1]1[CH:5]=[C:4]([C:6]([OH:8])=[O:7])[N:3]=[CH:2]1
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참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 27827431,2-Difluoro-4-(methylsulfonyl)benzeneHCID 178524800HCID 178524800, 화합물

생성물 1

HCID 710937501-(2-Fluoro-4-methanesulfonylphenyl)-1H-imidazole-4-carboxylic acid

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
120 °C

실험 절차

A mixture of 1H-imidazole-4-carboxylic acid (500 mg), 1,2-difluoro-4-methanesulfonylbenzene (1.2 g), and N,N-diisopropyl-ethyl-amine (4 mL) in N,N-dimethylformamide (6 mL) is heated to 120° C. overnight. The crude product is purified by HPLC. LC (method 20): tR=1.69 min; Mass spectrum (APCI): m/z=285 [M+H]+.

후처리

  1. customThe crude product is purified by HPLC

출처 및 근거

ORD 기록
ord-3ed85d0efecc41b0a3b6ab6f27e9acf9
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921398B2

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