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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-carbamic acid tert-butyl ester → (3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-amine

HRID 1691546
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HRID 1691546 반응식
C(OC(=O)[N:7]([CH2:18][C:19]1[CH:24]=[CH:23][C:22]([F:25])=[C:21]([F:26])[CH:20]=1)[C:8]1[S:12][C:11]2[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=2[C:9]=1[CH3:17])(C)(C)C>ClCCl.FC(F)(F)C(O)=O>[F:26][C:21]1[CH:20]=[C:19]([CH:24]=[CH:23][C:22]=1[F:25])[CH2:18][NH:7][C:8]1[S:12][C:11]2[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=2[C:9]=1[CH3:17]
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참가 물질

4

반응물 1

HCID 57920462(3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-carbamic acid tert-butyl ester

생성물 1

HCID 57920455(3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-amine

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of compound 125-C (2.7 g, 6.9 mmol) in dichloromethane (40 mL) and trifluoroacetic acid (40 mL) was stirred at rt for 4 h. The solvent was evaporated in vacuo, and the residue partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The organic layer was dried over sodium sulfate, and the solvent evaporated in vacuo to afford compound 125-D as a colorless solid (1.86 g, 93%). 1H-NMR (CDCl3): δ 2.16 (s, 3H), 4.37 (s, 2H), 7.09-7.32 (m, 5H), 7.40 (d, 1H), 7.60 (d, 1H); MS: m/z 290.1 (MH+).

후처리

  1. customThe solvent was evaporated in vacuo
  2. customthe residue partitioned between dichloromethane and saturated aqueous sodium bicarbonate
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. customthe solvent evaporated in vacuo
  5. customto afford compound 125-D as a colorless solid (1.86 g, 93%)

출처 및 근거

ORD 기록
ord-97ea309fd5124e5b9f45915ea87a92eb
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08153682B2

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