Sodium hydride → 2-Dimethylsulphamoyl-7-fluoro-10-(3-(4-methylpiperazin-1-yl)propyl)phenothiazine

HRID 1659092ノート

反応式

HRID 1659092 の反応式
[CH3:1][N:2]([CH3:21])[S:3]([C:6]1[CH:19]=[CH:18][C:17]2[S:16][C:15]3[C:10](=[CH:11][CH:12]=[C:13]([F:20])[CH:14]=3)[NH:9][C:8]=2[CH:7]=1)(=[O:5])=[O:4].[H-].[Na+].Cl[CH2:25][CH2:26][CH2:27][N:28]1[CH2:33][CH2:32][N:31]([CH3:34])[CH2:30][CH2:29]1>CN(C)C=O>[CH3:1][N:2]([CH3:21])[S:3]([C:6]1[CH:19]=[CH:18][C:17]2[S:16][C:15]3[C:10](=[CH:11][CH:12]=[C:13]([F:20])[CH:14]=3)[N:9]([CH2:25][CH2:26][CH2:27][N:28]3[CH2:33][CH2:32][N:31]([CH3:34])[CH2:30][CH2:29]3)[C:8]=2[CH:7]=1)(=[O:4])=[O:5]

参加物

5

実験手順

12 grams of N,N-dimethyl-7-fluoro-phenothiazine-2-sulphonamide were dissolved in 50 milliliters of dry dimethylformamide, 1.9 grams of 50% sodium hydride in oil added and the mixture stirred for 1 hour. 7.2 grams of 1-(3-chloropropyl)-4-methylpiperazine were then added and the mixture heated for two hours on a steam bath. Then the mixture was poured onto crushed ice, the resulting mixture extracted with ether, the ether phase washed, dried over anhydrous magnesium sulphate and the ether evaporated. 13 grams of 2-dimethylsulphamoyl-7-fluoro-10-(3-(4-methylpiperazin-1-yl)propyl)phenothiazine was thus obtained as a yellow oil. The dimaleate was made from an ethanol solution of the base and melted at 166°-169° Centigrade.

後処理

  1. temperaturethe mixture heated for two hours on a steam bath
  2. additionThen the mixture was poured
  3. customonto crushed ice
  4. extractionthe resulting mixture extracted with ether
  5. washthe ether phase washed
  6. dry with materialdried over anhydrous magnesium sulphate
  7. customthe ether evaporated

出典と根拠

ORDレコード
ord-0d47f33e0502409cb18c6acaab985618
出典データセット
uspto-grants-1976_06
特許番号
US03966930

反応ノート

読み込み中…