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Methanol → 5-(4-Hydroxymethylbenzoyl)-3-thiophene sulfonamide

HRID 1463259
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인쇄 미리보기

반응식

HRID 1463259 반응식
C([O:4][CH2:5][C:6]1[CH:22]=[CH:21][C:9]([C:10]([C:12]2[S:16][CH:15]=[C:14]([S:17]([NH2:20])(=[O:19])=[O:18])[CH:13]=2)=[O:11])=[CH:8][CH:7]=1)(=O)C.C([O-])([O-])=O.[K+].[K+].CO>C(OCC)(=O)C>[OH:4][CH2:5][C:6]1[CH:22]=[CH:21][C:9]([C:10]([C:12]2[S:16][CH:15]=[C:14]([S:17]([NH2:20])(=[O:19])=[O:18])[CH:13]=2)=[O:11])=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 11430Potassium CarbonateHCID 107595215-(4-Acetoxymethylbenzoyl)-3-thiophene sulfonamide

생성물 1

HCID 108278525-(4-Hydroxymethylbenzoyl)-3-thiophene sulfonamide수율 0.1%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

14 mg (41.3 mmol) of 5-(4-acetoxymethylbenzoyl)-3-thiophene sulfonamide and 9 mg (61.8 mmol) of K2CO3 were added to 3 mL of methanol. After stirring at rt for 11 h the solution was diluted with ethyl acetate and washed with 1N HCl followed with water (2×) and brine. The solvent was removed under vacuum to afford 12.5 mg of 5-(4-hydroxymethylbenzoyl)-3-thiophene sulfonamide as a white solid.

후처리

  1. washwashed with 1N HCl
  2. customThe solvent was removed under vacuum

출처 및 근거

ORD 기록
ord-7e2976f93b13410196410fba2c02cf85
출처 데이터셋
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05300499

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