Potassium Carbonate → Cediranib

HRID 2263484ノート

反応式

HRID 2263484 の反応式
[F:1][C:2]1[C:10]([O:11][C:12]2[C:21]3[C:16](=[CH:17][C:18](O)=[C:19]([O:22][CH3:23])[CH:20]=3)[N:15]=[CH:14][N:13]=2)=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:25])[NH:6]2.[C:26](=[O:29])([O-])[O-].[K+].[K+].[C:32](OC)([CH3:35])([CH3:34])C>CN1CCCC1=O>[F:1][C:2]1[C:10]([O:11][C:12]2[C:21]3[C:16](=[CH:17][C:18]([O:29][CH2:26][CH2:4][CH2:5][N:6]4[CH2:35][CH2:32][CH2:34][CH2:7]4)=[C:19]([O:22][CH3:23])[CH:20]=3)[N:15]=[CH:14][N:13]=2)=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:25])[NH:6]2

参加物

5

反応条件

温度
80 °C

実験手順

To a solution of 4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxyquinazolin-7-ol (2.5 g) in 1-methyl-2-pyrrolidinone (25 ml) and methyl tert-butyl ether (1.8 ml) was added potassium carbonate (815 mg). The mixture was degassed by holding under vacuum and letting down with nitrogen. This was carried out five times. The mixture was heated to 80° C. and 4-azoniaspiro[3,4]octane bromide (1.75 g) was added. The mixture was maintained at 80° C. for 3.5 hours. To the hot mixture was added water (27 ml) over 2 hours. The mixture was cooled to 64° C. and the solid filtered. The solid was washed with 1:1 v/v 1-methyl-2-pyrrolidinone/water (5 ml) and then water (4×5 ml). The solid was dried in a vacuum oven to give 4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline.

後処理

  1. customThe mixture was degassed
  2. addition4-azoniaspiro[3,4]octane bromide (1.75 g) was added
  3. temperatureThe mixture was maintained at 80° C. for 3.5 hours
  4. additionTo the hot mixture was added water (27 ml) over 2 hours
  5. temperatureThe mixture was cooled to 64° C.
  6. filtrationthe solid filtered
  7. washThe solid was washed with 1:1 v/v 1-methyl-2-pyrrolidinone/water (5 ml)
  8. customThe solid was dried in a vacuum oven

出典と根拠

ORDレコード
ord-af4bedf7b4a14ab0adc74270cf29356d
出典データセット
uspto-grants-2010_12
特許番号
US07851623B2

反応ノート

読み込み中…