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2-(2-Methoxy-3-nitro-phenyl)-5-methyl-thiazole-4-carboxylic acid → HCID 57483840, 화합물

HRID 384389
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인쇄 미리보기

반응식

HRID 384389 반응식
[CH3:1][O:2][C:3]1[C:8]([N+:9]([O-])=O)=[CH:7][CH:6]=[CH:5][C:4]=1[C:12]1[S:13][C:14]([CH3:20])=[C:15]([C:17]([OH:19])=[O:18])[N:16]=1>CO.[Pd]>[CH3:1][O:2][C:3]1[C:8]([NH2:9])=[CH:7][CH:6]=[CH:5][C:4]=1[C:12]1[S:13][C:14]([CH3:20])=[C:15]([C:17]([OH:19])=[O:18])[N:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 574838392-(2-Methoxy-3-nitro-phenyl)-5-methyl-thiazole-4-carboxylic acid

생성물 1

HCID 57483840HCID 57483840, 화합물수율 92.7%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

2-(2-Methoxy-3-nitro-phenyl)-5-methyl-thiazole-4-carboxylic acid 47a (300 mg, 1.02 mmol) was dissolved in 15 mL of methanol followed by addition of 30 mg of palladium on carbon. The reaction mixture was stirred for 24 hours under hydrogen atmosphere. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered to remove palladium on carbon and the filtrate was concentrated under reduced pressure to obtain the title compound 2-(2-methoxy-3-amino-phenyl)-5-methyl-thiazole-4-carboxylic acid 47b (250 mg, yield 92%) as a yellow solid.

후처리

  1. filtrationThe mixture was filtered
  2. customto remove palladium on carbon
  3. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-a5cddb36a3394ef9a452d8b29562aaa5
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367710B2

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