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Hydrogen Bromide → HCID 136117081, 화합물

HRID 384390
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인쇄 미리보기

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HRID 384390 반응식
C[O:2][C:3]1[C:8]([NH2:9])=[CH:7][CH:6]=[CH:5][C:4]=1[C:10]1[S:11][C:12]([CH3:18])=[C:13]([C:15]([OH:17])=[O:16])[N:14]=1.[BrH:19]>>[BrH:19].[OH:2][C:3]1[C:8]([NH2:9])=[CH:7][CH:6]=[CH:5][C:4]=1[C:10]1[S:11][C:12]([CH3:18])=[C:13]([C:15]([OH:17])=[O:16])[N:14]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 260Hydrogen BromideHCID 57483840HCID 57483840, 화합물

생성물 1

HCID 136117081HCID 136117081, 화합물수율 64%

반응 조건

온도
80 °C

실험 절차

2-(2-Methoxy-3-amino-phenyl)-5-methyl-thiazole-4-carboxylic acid 47b (280 mg, 0.94 mmol) was dissolved in 5 mL of hydrogen bromide. The reaction mixture was stirred overnight at 80° C. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filter cake was washed with ethyl acetate and dried to obtain the title compound 2-(2-hydroxy-3-amino-phenyl)-5-methyl-thiazole-4-carboxylic acid hydrobromide 47c (200 mg, yield 64%) as a yellow solid.

후처리

  1. filtrationThe mixture was filtered
  2. wash
the filter cake was washed with ethyl acetate
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-a9f5085a6caf440b96b70213ded2655e
    출처 데이터셋
    uspto-grants-2013_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08367710B2

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