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Trifluoroacetic acid → HCID 44818005, 화합물

HRID 390051
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HRID 390051 반응식
CC([N:5]([CH2:9][CH2:10][CH2:11][NH:12][C:13]1[N:14]=[C:15]([NH:24][C:25]2[CH:30]=[CH:29][CH:28]=[C:27]([CH3:31])[CH:26]=2)[C:16]2[C:22](=[O:23])[NH:21][CH:20]=[CH:19][C:17]=2[N:18]=1)C(=O)[O-])(C)C.C(O)(C(F)(F)F)=O>ClCCl>[NH2:5][CH2:9][CH2:10][CH2:11][NH:12][C:13]1[N:14]=[C:15]([NH:24][C:25]2[CH:30]=[CH:29][CH:28]=[C:27]([CH3:31])[CH:26]=2)[C:16]2[C:22](=[O:23])[NH:21][CH:20]=[CH:19][C:17]=2[N:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 86654202HCID 86654202, 화합물

생성물 1

HCID 44818005HCID 44818005, 화합물수율 133.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1,1-dimethylethyl[3-({4-[(3-methylphenyl)amino]-5-oxo-5,6-dihydropyrido[4,3-d]pyrimidin-2-yl}amino)propyl]carbamate (245 mg, 0.577 mmol) was dissolved into dichloromethane (3 mL) and TFA (1 mL) was added. The reaction mixture was stirred for 1 h and concentrated. The residue was further dried under high vacuum to afford the product as a TFA salt (250 mg).

후처리

  1. additionwas added
  2. concentrationconcentrated
  3. customThe residue was further dried under high vacuum

출처 및 근거

ORD 기록
ord-2396b788e5b54b66b2380d554709662b
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08383635B2

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