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4-Amino-3,5-dimethylisoxazole → 7-Difluoromethoxy-2-ethylfuro[2,3-c]pyridine-4-carboxylic acid (3,5-dimethylisoxazol-4-yl)amide

HRID 564744
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인쇄 미리보기

반응식

HRID 564744 반응식
[N+](C1C=CC(O[C:11]([C:13]2[C:14]3[CH:25]=[C:24]([CH2:26][CH3:27])[O:23][C:15]=3[C:16]([O:19][CH:20]([F:22])[F:21])=[N:17][CH:18]=2)=[O:12])=CC=1)([O-])=O.[CH3:28][C:29]1[C:33]([NH2:34])=[C:32]([CH3:35])[O:31][N:30]=1>>[CH3:28][C:29]1[C:33]([NH:34][C:11]([C:13]2[C:14]3[CH:25]=[C:24]([CH2:26][CH3:27])[O:23][C:15]=3[C:16]([O:19][CH:20]([F:21])[F:22])=[N:17][CH:18]=2)=[O:12])=[C:32]([CH3:35])[O:31][N:30]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 1820404-Amino-3,5-dimethylisoxazoleHCID 538910297-Difluoromethoxy-2-ethylfuro[2,3-c]pyridine-4-carboxylic acid 4-nitrophenyl ester

생성물 1

HCID 536439207-Difluoromethoxy-2-ethylfuro[2,3-c]pyridine-4-carboxylic acid (3,5-dimethylisoxazol-4-yl)amide수율 9.7%

실험 절차

This Example was conducted following the procedure of Example 1, but starting from 7-difluoromethoxy-2-ethylfuro[2,3-c]pyridine-4-carboxylic acid 4-nitrophenyl ester (200 mg) and 3,5-dimethylisoxazol-4-ylamine (118 mg). Purification by column chromatography on silica eluting with 30% ethyl acetate in hexane followed by trituration in diethyl ether afforded the title compound as an off-white solid (18 mg).

후처리

  • customPurification by column chromatography on silica eluting with 30% ethyl acetate in hexane
  • 출처 및 근거

    ORD 기록
    ord-42b416664123486b978dc326609796b3
    출처 데이터셋
    uspto-grants-2001_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06169090A

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