Cesium carbonate → HCID 70169281, 화합물

HRID 1426984

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HRID 1426984 반응식
Cl[CH2:2][C@@H:3]([OH:31])[CH2:4][NH:5][C:6]([C:8]1[CH:9]=[N:10][N:11]2[CH:16]=[CH:15][C:14]([N:17]3[CH2:21][CH:20]([OH:22])[CH2:19][C@@H:18]3[C:23]3[CH:28]=[C:27]([F:29])[CH:26]=[CH:25][C:24]=3[OH:30])=[N:13][C:12]=12)=[O:7].C([O-])([O-])=O.[Cs+].[Cs+]>CN(C=O)C>[F:29][C:27]1[CH:26]=[CH:25][C:24]2[O:30][CH2:2][C@@H:3]([OH:31])[CH2:4][NH:5][C:6](=[O:7])[C:8]3=[C:12]4[N:13]=[C:14]([CH:15]=[CH:16][N:11]4[N:10]=[CH:9]3)[N:17]3[C@H:18]([CH2:19][C@@H:20]([OH:22])[CH2:21]3)[C:23]=2[CH:28]=1

참가 물질

4

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온도
85 °C

실험 절차

A mixture of N-((S)-3-chloro-2-hydroxypropyl)-5-((R)-2-(5-fluoro-2-hydroxyphenyl)-4-hydroxypyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide (0.0407 g, 0.0778 mmol) and Cs2CO3 (0.127 g, 0.389 mmol) in DMF (3.6 mL) was heated at 85° C. for 30 minutes. The reaction mixture was cooled to ambient temperature and filtered. The filtrate was concentrated under reduced pressure to give the crude material which was purified by silica column chromatography, eluting with 0-20% MeOH/EtOAc to afford the crude product. The crude material was purified using chiral column chromatography (Chiral Tech OD-H column, 20% EtOH in hexanes). Isolation of the material having a retention time of about 21.8 minutes afforded the title compound (0.0052 g, 16.2% yield). The stereochemistry of the title compound was confirmed by 1H-NMR nOe experiment. LC/MS (ES+APCI) m/z=414.1 (M+H).

후처리

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. filtrationfiltered
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. customto give the crude material which
  5. customwas purified by silica column chromatography
  6. washeluting with 0-20% MeOH/EtOAc
  7. customto afford the crude product
  8. customThe crude material was purified

출처 및 근거

ORD 기록
ord-33e093160c4c439cbd02921a921bfec5
출처 데이터셋
uspto-grants-2015_01
특허 번호
US08933084B2

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