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Trifluoroacetic acid → N-(3,3-difluorocyclobutyl)-3-(piperazin-1-ylmethyl)benzamide

HRID 1878434
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반응식

HRID 1878434 반응식
[F:1][C:2]1([F:29])[CH2:5][CH:4]([NH:6][C:7]([C:9]2[CH:10]=[C:11]([CH:26]=[CH:27][CH:28]=2)[CH2:12][N:13]2[CH2:18][CH2:17][N:16](C(OC(C)(C)C)=O)[CH2:15][CH2:14]2)=[O:8])[CH2:3]1.FC(F)(F)C(O)=O>ClCCl>[F:29][C:2]1([F:1])[CH2:5][CH:4]([NH:6][C:7](=[O:8])[C:9]2[CH:28]=[CH:27][CH:26]=[C:11]([CH2:12][N:13]3[CH2:14][CH2:15][NH:16][CH2:17][CH2:18]3)[CH:10]=2)[CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 57917660HCID 57917660, 화합물

생성물 1

HCID 57917681N-(3,3-difluorocyclobutyl)-3-(piperazin-1-ylmethyl)benzamide수율 81.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

tert-Butyl 4-(3-(3,3-difluorocyclobutylcarbamoyl)benzyl)piperazine-1-carboxylate (12.65 mmol, 5.179 g) was stirred at room temperature in dichloromethane (10 mL)/trifluoroacetic acid (10 mL) for 1 hour with sonication. The solvent was removed under vacuum and the resulting residue was purified by strong cation exchange column chromatography to afford the title compound (3.19 g). MS (ESI) m/z 310.4 [M+H]+

후처리

  1. customwith sonication
  2. customThe solvent was removed under vacuum
  3. customthe resulting residue was purified by strong cation exchange column chromatography

출처 및 근거

ORD 기록
ord-1becd9dc5c424d3aa0def01a9a8a43f0
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08314091B2

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