Cesium carbonate → benzyl ((1S,3R)-3-(pyrazin-2-ylamino)cyclohexyl)carbamate

HRID 75051

反応式

HRID 75051 の反応式
[NH2:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][C@H:4]([NH:8][C:9](=[O:18])[O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:3]1.C(=O)([O-])[O-].[Cs+].[Cs+].I[C:26]1[CH:31]=[N:30][CH:29]=[CH:28][N:27]=1.CC(C)C(C1CCCCC1=O)=O.C(=O)(O)[O-].[Na+]>CN(C=O)C.[Cu]I.C(OCC)(=O)C>[N:27]1[CH:28]=[CH:29][N:30]=[CH:31][C:26]=1[NH:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][C@H:4]([NH:8][C:9](=[O:18])[O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:3]1

参加物

9

実験手順

A suspension of CuI (0.006 g, 0.030 mmol), benzyl N-[(1S,3R)-3-aminocyclo-hexyl]carbamate, 18e, (0.075 g, 0.302 mmol) and cesium carbonate (0.197 g, 0.604 mmol) in DMF was evacuated and refilled with nitrogen multiple times. 2-iodopyrazine (0.036 mL, 0.362 mmol) and 2-(2-methylpropanoyl)cyclohexanone (0.020 mL g, 0.121 mmol) were then added and the reaction was stirred at room temperature overnight. The reaction was diluted into ethyl acetate and aqueous saturated sodium bicarbonate. The organic phase was separated, dried (MgSO4), filtered and concentrated in vacuo. The crude residue was purified by silica gel chromatography (0-10% MeOH/CH2Cl2) to afford 40 mg of the desired product as yellow solid.

後処理

  1. customwas evacuated
  2. additionrefilled with nitrogen multiple times
  3. customThe organic phase was separated
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe crude residue was purified by silica gel chromatography (0-10% MeOH/CH2Cl2)

出典と根拠

ORDレコード
ord-9b84f14b8bf940c9bf556156b1b98b6d
出典データセット
uspto-grants-2014_09
特許番号
US08829007B2

関連ノート

読み込み中…