Cesium carbonate → HCID 68750611, 화합물

HRID 406546

반응식

HRID 406546 반응식
C(=O)([O-])[O-].[Cs+].[Cs+].[C:7]([O:11][C:12]([NH:14][C@@H:15]([C:18]([O:20][CH3:21])=[O:19])[CH2:16]I)=[O:13])([CH3:10])([CH3:9])[CH3:8].[Cl:22][C:23]1[CH:24]=[C:25]([CH2:29][C:30](=[O:32])[CH3:31])[CH:26]=[CH:27][CH:28]=1>CN(C=O)C>[C:7]([O:11][C:12]([NH:14][CH:15]([CH2:16][CH:29]([C:25]1[CH:26]=[CH:27][CH:28]=[C:23]([Cl:22])[CH:24]=1)[C:30](=[O:32])[CH3:31])[C:18]([O:20][CH3:21])=[O:19])=[O:13])([CH3:10])([CH3:9])[CH3:8]

참가 물질

5

반응물 3

HCID 10796Cesium carbonate2회HCID 27340971-(3-Chlorophenyl)propan-2-oneHCID 11416215(S)-Methyl 2-Boc-amino-3-iodopropionate

생성물 1

HCID 68750611HCID 68750611, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of cesium carbonate (9.80 g, 30.1 mmol) and methyl N-(tert-butoxycarbonyl)-3-iodo-D-alaninate (9.90 g, 30.1 mmol) in DMF (75 mL) was stirred at 23° C. for 45 min before 1-(3-chlorophenyl)propan-2-one (6.09 g, 36.1 mmol) and additional cesium carbonate (9.80 g, 30.1 mmol) were added. The resulting mixture was stirred for 2.5 h. The majority of the DMF was then removed under reduced pressure at a bath temperature of <40° C. The concentrated mixture was partitioned between water (100 mL) and ethyl acetate (2×200 mL). The combined organic layers were washed with brine, dried over sodium sulfate and concentrated to give the title compound as a 1:1 racemic mixture of cis and trans diastereomers, which was used without further purification. MS: m/z=392.1 (M+Na).

후처리

  1. additionwere added
  2. customThe majority of the DMF was then removed under reduced pressure at a bath temperature of <40° C
  3. customThe concentrated mixture was partitioned between water (100 mL) and ethyl acetate (2×200 mL)
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8cba6807c7924f3e94d489f3cd54315a
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08754096B2

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