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Trifluoroacetic acid → 4-[7-(3-Imidazol-1-ylprop-1-ynyl)-3-oxo-2H-isoquinolin-2-ylmethyl]benzoic Acid

HRID 488787
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반응식

HRID 488787 반응식
C([O:5][C:6](=[O:33])[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][N:14]2[C:23](=[O:24])[CH:22]=[C:21]3[C:16]([CH:17]=[C:18]([C:25]#[C:26][CH2:27][N:28]4[CH:32]=[CH:31][N:30]=[CH:29]4)[CH:19]=[CH:20]3)=[CH:15]2)=[CH:9][CH:8]=1)(C)(C)C.FC(F)(F)C(O)=O>>[N:28]1([CH2:27][C:26]#[C:25][C:18]2[CH:19]=[CH:20][C:21]3[C:16]([CH:17]=2)=[CH:15][N:14]([CH2:13][C:10]2[CH:11]=[CH:12][C:7]([C:6]([OH:33])=[O:5])=[CH:8][CH:9]=2)[C:23](=[O:24])[CH:22]=3)[CH:32]=[CH:31][N:30]=[CH:29]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6422Trifluoroacetic acidHCID 104783554-[7-(3-Imidazol-1-ylprop-1-ynyl)-3-oxo-2H-isoquinolin-2-ylmethyl]benzoic Acid tert-butyl Ester

생성물 1

HCID 104076004-[7-(3-Imidazol-1-ylprop-1-ynyl)-3-oxo-2H-isoquinolin-2-ylmethyl]benzoic Acid

실험 절차

A solution of 4-[7-(3-imidazol-1-ylprop-1-ynyl)-3-oxo-2H-isoquinolin-2-ylmethyl]benzoic acid tert-butyl ester (0.38 g, 0.86 mmol, Example 13A) is treated with trifluoroacetic acid (6 mL) and stirred at room temperature for 30 minutes. The reaction mixture is evaporated to dryness, triturated with ethyl acetate, the solid is collected by filtration, washed with water, washed with ethyl acetate, and dried under house vacuum. This will afford the desired product.

후처리

  1. customThe reaction mixture is evaporated to dryness
  • customtriturated with ethyl acetate
  • filtrationthe solid is collected by filtration
  • washwashed with water
  • washwashed with ethyl acetate
  • customdried under house vacuum
  • 출처 및 근거

    ORD 기록
    ord-dc691778348542bb8cbfcc3ea7488fcf
    출처 데이터셋
    uspto-grants-2005_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06974822B2

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