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Trifluoroacetic acid → HCID 58864314, 화합물

HRID 2250178
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HRID 2250178 반응식
[CH3:1][O:2][C:3](=[O:27])[C:4]([NH:16]C(OCC1C=CC=CC=1)=O)=[CH:5][C:6]1[CH:7]=[C:8]2[C:12](=[C:13]([Cl:15])[CH:14]=1)[NH:11][N:10]=[CH:9]2.FC(F)(F)C(O)=O>CO>[CH3:1][O:2][C:3](=[O:27])[CH:4]([NH2:16])[CH2:5][C:6]1[CH:7]=[C:8]2[C:12](=[C:13]([Cl:15])[CH:14]=1)[NH:11][N:10]=[CH:9]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 68707452Methyl 3-(7-chloro-1H-indazol-5-yl)-2-[[(phenylmethoxy)carbonyl]amino]-2-propenoate

생성물 1

HCID 58864314HCID 58864314, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 2-benzyloxycarbonylamino-3-(7-chloro-1H-indazol-5-yl)-acrylic acid methyl ester (300 mg, 0.78 mmol) in methanol (10 mL) was treated with trifluoroacetic acid (0.2 mL), flushed with nitrogen, and treated with 10% palladium on charcoal (30 mg). The flask was flushed with hydrogen and allowed to stir under an atmosphere of hydrogen. After 4 days, all starting material had been consumed. The reaction was flushed with nitrogen, filtered through celite, and concentrated. Column chromatography gave 78 mg (40%).

후처리

  1. customflushed with nitrogen
  2. additiontreated with 10% palladium on charcoal (30 mg)
  3. customThe flask was flushed with hydrogen
  4. customall starting material had been consumed
  5. customThe reaction was flushed with nitrogen
  6. filtrationfiltered through celite
  7. concentrationconcentrated
  8. customColumn chromatography gave 78 mg (40%)

출처 및 근거

ORD 기록
ord-c12ff2d671b04920bf629e7490557933
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07314883B2

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