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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → (S)-1-(2-{4-[5-(2,5-difluorophenoxy)-7-propoxyoxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethylphenoxy}acetyl)pyrrolidine-2-carboxylic acid

HRID 81506
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HRID 81506 반응식
[F:1][C:2]1[CH:45]=[CH:44][C:43]([F:46])=[CH:42][C:3]=1[O:4][C:5]1[N:6]=[C:7]([O:38][CH2:39][CH2:40][CH3:41])[C:8]2[N:13]=[C:12]([C:14]3[CH:35]=[C:34]([CH3:36])[C:17]([O:18][CH2:19][C:20]([N:22]4[CH2:26][CH2:25][CH2:24][C@H:23]4[C:27]([O:29]C(C)(C)C)=[O:28])=[O:21])=[C:16]([CH3:37])[CH:15]=3)[O:11][C:9]=2[N:10]=1.FC(F)(F)C(O)=O>ClCCl>[F:1][C:2]1[CH:45]=[CH:44][C:43]([F:46])=[CH:42][C:3]=1[O:4][C:5]1[N:6]=[C:7]([O:38][CH2:39][CH2:40][CH3:41])[C:8]2[N:13]=[C:12]([C:14]3[CH:35]=[C:34]([CH3:36])[C:17]([O:18][CH2:19][C:20]([N:22]4[CH2:26][CH2:25][CH2:24][C@H:23]4[C:27]([OH:29])=[O:28])=[O:21])=[C:16]([CH3:37])[CH:15]=3)[O:11][C:9]=2[N:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 86688233tert-Butyl(S)-1-(2-{4-[5-(2,5-difluorophenoxy)-7-propoxyoxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethylphenoxy}acetyl)pyrrolidine-2-carboxylate

생성물 1

HCID 53311961(S)-1-(2-{4-[5-(2,5-difluorophenoxy)-7-propoxyoxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethylphenoxy}acetyl)pyrrolidine-2-carboxylic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

59 mg of tert-butyl(S)-1-(2-{4-[5-(2,5-difluorophenoxy)-7-propoxyoxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethylphenoxy}acetyl)pyrrolidine-2-carboxylate were dissolved in 1.2 ml of dichloromethane, and 0.5 ml of trifluoroacetic acid was added. After 16 h at room temperature, the mixture was concentrated under reduced pressure and freeze-dried. This gave 53 mg of the title compound.

후처리

  1. concentrationthe mixture was concentrated under reduced pressure
  2. customfreeze-dried

출처 및 근거

ORD 기록
ord-da6002ff44434dd6b48c3c07d9258a0f
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846691B2

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