Water → HCID 70464043、化合物

HRID 543544

反応式

HRID 543544 の反応式
CC(O[CH2:5][C:6]1[CH2:15][S:14][C@@H:9]2[C@H:10]([NH2:13])[C:11](=[O:12])[N:8]2[C:7]=1[C:16]([OH:18])=[O:17])=O.O.[CH3:20][N:21]([CH3:31])[C:22]([CH2:24][C:25]1[S:26][C:27]([SH:30])=[N:28][N:29]=1)=[O:23].P(Cl)(Cl)(OP(Cl)(Cl)=O)=O>C(#N)C>[NH2:13][CH:10]1[C:11](=[O:12])[N:8]2[C:7]([C:16]([OH:18])=[O:17])=[C:6]([CH2:5][S:30][C:27]3[S:26][C:25]([CH2:24][C:22]([N:21]([CH3:20])[CH3:31])=[O:23])=[N:29][N:28]=3)[CH2:15][S:14][C@H:9]12

参加物

6

反応条件

温度
10 °C

実験手順

Mixed were 1.36 g of 7-ACA, 0.36 g of water and 1.32 g of 2-dimethylaminocarbonylmethyl-5-mercapto-1,3,4-thiadiazole, and 6.5 ml of acetonitrile was added. 5.04 g of diphosphoryl tetrachloride was added through a dropping funnel to the mixture at -20° to -30° C., followed by rinsing the funnel with 1.5 ml of acetonitrile. The reaction mixture was warmed at 10° C. over a period of 5 minutes with stirring, placed in a warm water bath of 40° C. and stirred at the same temperature for 20 minutes. The reaction solution was cooled with ice and adjusted to pH 4.1 with aqueous concentrated ammonia after the addition of 10 ml of cold water. The precipitate was recovered by filtration, washed with water and dried, thereby affording 1.82 g (87.6%) of 7-amino-3-(2-dimethylaminocarbonylmethyl-1,3,4-thiadiazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid.

後処理

  1. additionMixed
  2. additionwas added
  3. washby rinsing the funnel with 1.5 ml of acetonitrile
  4. customplaced in a warm water bath of 40° C.
  5. stirringstirred at the same temperature for 20 minutes
  6. temperatureThe reaction solution was cooled with ice
  7. additionafter the addition of 10 ml of cold water
  8. filtrationThe precipitate was recovered by filtration
  9. washwashed with water
  10. customdried

出典と根拠

ORDレコード
ord-d0bc62e7a509467b8b3f405fab019620
出典データセット
uspto-grants-1984_05
特許番号
US04446318

関連ノート

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