1,1'-Carbonyldiimidazole → (2S,4S)-4-(8-chloro-2-(4-isopropylthiazol-2-yl)-7-methoxyquinolin-4-yloxy)-N-(hex-5-enyl)-1-(1H-imidazole-1-carbonyl)-N-methylpyrrolidine-2-carboxamide

HRID 420093ノート

反応式

HRID 420093 の反応式
Cl.[Cl:2][C:3]1[C:4]([O:37][CH3:38])=[CH:5][CH:6]=[C:7]2[C:12]=1[N:11]=[C:10]([C:13]1[S:14][CH:15]=[C:16]([CH:18]([CH3:20])[CH3:19])[N:17]=1)[CH:9]=[C:8]2[O:21][C@@H:22]1[CH2:26][NH:25][C@H:24]([C:27]([N:29]([CH2:31][CH2:32][CH2:33][CH2:34][CH:35]=[CH2:36])[CH3:30])=[O:28])[CH2:23]1.[C:39](N1C=CN=C1)([N:41]1[CH:45]=[CH:44][N:43]=[CH:42]1)=[O:40]>ClCCl>[Cl:2][C:3]1[C:4]([O:37][CH3:38])=[CH:5][CH:6]=[C:7]2[C:12]=1[N:11]=[C:10]([C:13]1[S:14][CH:15]=[C:16]([CH:18]([CH3:20])[CH3:19])[N:17]=1)[CH:9]=[C:8]2[O:21][C@@H:22]1[CH2:26][N:25]([C:39]([N:41]2[CH:45]=[CH:44][N:43]=[CH:42]2)=[O:40])[C@H:24]([C:27]([N:29]([CH2:31][CH2:32][CH2:33][CH2:34][CH:35]=[CH2:36])[CH3:30])=[O:28])[CH2:23]1

参加物

4

実験手順

Compound 135 (10 g) was dissolved in anhydrous dichloromethane (20 mL) under argon. 1,1′-Carbonyldiimidazole (2 eq.) was added at room temperature. The reaction mixture was stirred for 45 min. The mixture was diluted with DCM, washed with water, dried over Na2SO4, and concentrated under vacuum. Compound 136 (9.9 g) was recovered as an off-white foam in 99% yield and in 98% purity (HPLC).

後処理

  1. washwashed with water
  2. dry with materialdried over Na2SO4
  3. concentrationconcentrated under vacuum
  4. customCompound 136 (9.9 g) was recovered as an off-white foam in 99% yield and in 98% purity (HPLC)

出典と根拠

ORDレコード
ord-e2bd2437792049e48cf9302f67842b71
出典データセット
uspto-grants-2012_01
特許番号
US08093379B2

反応ノート

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