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2-(Benzylamino)-5-(trifluoromethyl)benzenesulfonamide → HCID 11333908, 화합물

HRID 1066162
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인쇄 미리보기

반응식

HRID 1066162 반응식
C([NH:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][C:10]=1[S:19]([NH2:22])(=[O:21])=[O:20])C1C=CC=CC=1.[H][H]>CO.[Pd]>[NH2:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]([F:17])([F:16])[F:18])=[CH:11][C:10]=1[S:19]([NH2:22])(=[O:21])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 112443972-(Benzylamino)-5-(trifluoromethyl)benzenesulfonamideHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 11333908HCID 11333908, 화합물수율 94.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A solution of 2-benzylamino-5-trifluoromethylbenzenesulfonamide (7.3 g) in methanol (80 mL) was supplemented with 10% Pd/C (0.73 g) and submitted to hydrogen under pressure (4 bars) during 90 min. at room temperature. The insoluble material was removed by filtration and the filtrate was concentrated to dryness. The residue was crystallized in methanol-water to give the title compound (yield: 5 g); m.p. 142-143° C.

후처리

  1. customThe insoluble material was removed by filtration
  2. concentrationthe filtrate was concentrated to dryness
  3. customThe residue was crystallized in methanol-water

출처 및 근거

ORD 기록
ord-61f40d3017aa402187936c8fcb603b2f
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06242443B1

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