Hydrochloric Acid → 2',3'-di-O-methoxycarbonyl-5'-deoxy-5-fluoro-N4-(pentyloxycarbonyl) cytidine

HRID 420837ノート

反応式

HRID 420837 の反応式
[CH3:1][O:2][C:3]([O:5][C@@H:6]1[C@H:10]([O:11][C:12]([O:14][CH3:15])=[O:13])[C@@H:9]([CH3:16])[O:8][C@H:7]1[N:17]1[CH:24]=[C:23]([F:25])[C:21]([NH2:22])=[N:20][C:18]1=[O:19])=[O:4].N1C=CC=CC=1.Cl[C:33]([O:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40])=[O:34].Cl>ClCCl>[CH3:1][O:2][C:3]([O:5][C@@H:6]1[C@H:10]([O:11][C:12]([O:14][CH3:15])=[O:13])[C@@H:9]([CH3:16])[O:8][C@H:7]1[N:17]1[CH:24]=[C:23]([F:25])[C:21]([NH:22][C:33]([O:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40])=[O:34])=[N:20][C:18]1=[O:19])=[O:4]

参加物

6

反応条件

温度
-2.5 °C

実験手順

35.8 g (0.099 mole) of the compound obtained in Example 2 was mixed with 163 ml of dichloromethane and 11 ml (0.136 mole) of pyridine, and stirred. After cooling the resulting mixture to −5 to 0° C., 15.7 ml (0.109 mole) of n-pentyl chloroformate was added dropwise thereto while maintaining the temperature of the reaction mixture at less than 0° C., followed adding the resulting mixture was warmed to room temperature and stirred for 2 hrs, 1 N HCl thereto. The organic layer was separated, successively washed with 163 ml of saturated sodium bicarbonate and 163 ml of water, dried over anhydrous sodium sulfate, and concentrated under a reduced pressure, to obtain 42.9 g of the title compound.

後処理

  1. temperaturewhile maintaining the temperature of the reaction mixture at less than 0° C.
  2. additionfollowed adding the resulting mixture
  3. temperaturewas warmed to room temperature
  4. stirringstirred for 2 hrs
  5. customThe organic layer was separated
  6. washsuccessively washed with 163 ml of saturated sodium bicarbonate and 163 ml of water
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated under a reduced pressure

出典と根拠

ORDレコード
ord-1cbe1ce39d054b469a44e82153c6c608
出典データセット
uspto-grants-2012_01
特許番号
US08097706B2

反応ノート

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