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Trifluoroacetic acid → HCID 57537545, 화합물

HRID 1693714
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HRID 1693714 반응식
[Br:1][C:2]1[C:3]([Cl:31])=[C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[CH2:17][O:18]C(C)(C)C)=[CH:9][N:8](COCC[Si](C)(C)C)[C:5]2=[N:6][CH:7]=1.FC(F)(F)C(O)=O>ClCCl>[Br:1][C:2]1[C:3]([Cl:31])=[C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[CH2:17][OH:18])=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 57537528HCID 57537528, 화합물

생성물 1

HCID 57537545HCID 57537545, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
23 °C

실험 절차

5-Bromo-3-(2-tert-butoxymethyl-phenyl)-4-chloro-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrrolo[2,3-b]pyridine (66 mg, 0.12 mmol) was dissolved in dichloromethane (1 mL) and trifluoroacetic acid (1 mL) and stirred at 23° C. for 15 h. The solvent was evaporated and the resulting oil was dissolved in methanol (1 mL) and ethylenediamine (0.2 mL) and stirred at 23° C. for 1 h. The mixture was concentrated to afford [2-(5-Bromo-4-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-phenyl]-methanol which was used in the next step without further purification.

후처리

  1. customThe solvent was evaporated
  2. dissolutionthe resulting oil was dissolved in methanol (1 mL)
  3. concentrationThe mixture was concentrated

출처 및 근거

ORD 기록
ord-1d4cafec7a3b46b3aaf824db02bee9ff
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158647B2

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