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Cesium carbonate → HCID 89581860、化合物

HRID 1474692
ノート
印刷プレビュー

反応式

HRID 1474692 の反応式
[NH:1]1[CH2:6][CH2:5][CH:4]([C@H:7]2[CH2:9][C@H:8]2[CH2:10][CH2:11][OH:12])[CH2:3][CH2:2]1.C(=O)([O-])[O-].[Cs+].[Cs+].Cl[C:20]1[N:25]=[CH:24][C:23]([O:26][CH3:27])=[CH:22][N:21]=1>CN(C=O)C.CCOC(C)=O>[CH3:27][O:26][C:23]1[CH:22]=[N:21][C:20]([N:1]2[CH2:6][CH2:5][CH:4]([C@H:7]3[CH2:9][C@H:8]3[CH2:10][CH2:11][OH:12])[CH2:3][CH2:2]2)=[N:25][CH:24]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 10796Cesium carbonateHCID 5890582-Chloro-5-methoxypyrimidineHCID 867111782-((1S,2R)-2-(piperidin-4-yl)cyclopropyl)ethanol

生成物 1

HCID 89581860HCID 89581860、化合物

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

2-((1S,2R)-2-(Piperidin-4-yl)cyclopropyl)ethanol (2.5 g, 14.77 mmol) was dissolved in DMF (30 ml) at RT under N2 and cesium carbonate (7.22 g, 22.15 mmol) was added. The mixture was stirred at RT for 5 min and 2-chloro-5-methoxypyrimidine (2.56 g, 17.72 mmol) was added. The mixture was stirred at 100° C. overnight. The mixture was diluted with EtOAc (100 ml), washed with sat. NH4Cl (100 ml), dried over MgSO4, and the concentrated in vacuo. The crude material was purified by silica gel column (100 g SNAP, 2060% EtOAc in hexane) to afford the title compound as a white solid. LC/MS (m/z): 278 (M+H)+. Rf was 0.4 @ 50% EtOAc in hexanes (blue spot on CAM stain).

後処理

  1. stirringThe mixture was stirred at 100° C. overnight
  2. washwashed with sat. NH4Cl (100 ml)
  3. dry with materialdried over MgSO4
  4. concentrationthe concentrated in vacuo
  5. customThe crude material was purified by silica gel column (100 g SNAP, 2060% EtOAc in hexane)

出典と根拠

ORDレコード
ord-b68b0e1702354c02ad56628fbbafeb13
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09018224B2

反応ノート

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