Methanol → Maribavir

HRID 381650ノート

反応式

HRID 381650 の反応式
[Cl:1][C:2]1[C:32]([Cl:33])=[CH:31][C:5]2[N:6]([C@H:13]3[O:25][C@@H:24]([CH2:26][O:27]C(=O)C)[C@H:19]([O:20]C(=O)C)[C@@H:14]3[O:15]C(=O)C)[C:7]([NH:9][CH:10]([CH3:12])[CH3:11])=[N:8][C:4]=2[CH:3]=1.C(=O)([O-])[O-].[Na+].[Na+].O.CO>C(O)C>[Cl:1][C:2]1[C:32]([Cl:33])=[CH:31][C:5]2[N:6]([C@H:13]3[O:25][C@@H:24]([CH2:26][OH:27])[C@H:19]([OH:20])[C@@H:14]3[OH:15])[C:7]([NH:9][CH:10]([CH3:11])[CH3:12])=[N:8][C:4]=2[CH:3]=1

参加物

6

実験手順

5,6-Dichloro-2-(isopropylamino)1-(2,3,5-tri-O-acetyl-beta-L-ribofuranosyl)-1H-benzimidazole (7.50 g, 14.93 mmol), sodium carbonate (1.72 g, 16.23 mmol), water (29 mL), methanol (100 mL) and ethanol (100 mL) were used according to general procedure III. The product was purified by silica gel chromatography using 55:45 dichloromethane/methanol to afford 4.72 g (84%) of a white foam. Analytical data were consistent with the assigned structure.

後処理

  1. customThe product was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-43f085f8073548f98f85e295d7ea6e24
出典データセット
uspto-grants-2001_10
特許番号
US06307043B1

反応ノート

読み込み中…