Hydrochloric Acid → (S)-8-chloro-9-oxo-11,12,13,13a-tetrahydro-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-thiocarboxamide

HRID 867541ノート

反応式

HRID 867541 の反応式
[Cl:1][C:2]1[C:7]2[C:8](=[O:21])[N:9]3[CH2:20][CH2:19][CH2:18][C@H:10]3[C:11]3[N:12]([CH:13]=[N:14][C:15]=3[C:16]#[N:17])[C:6]=2[CH:5]=[CH:4][CH:3]=1.C(N)(=[S:24])C.Cl.[OH-].[Na+]>O.CN(C)C=O>[Cl:1][C:2]1[C:7]2[C:8](=[O:21])[N:9]3[CH2:20][CH2:19][CH2:18][C@H:10]3[C:11]3[N:12]([CH:13]=[N:14][C:15]=3[C:16](=[S:24])[NH2:17])[C:6]=2[CH:5]=[CH:4][CH:3]=1

参加物

7

実験手順

20.0 g (67 mmol) of (S)-8-chloro-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carbonitrile and 10.06 g (134 mmol) of thioacetamide are heated to 90° together with 100 ml of dry N,N-dimethylformamide, whereupon the mixture is saturated with dry hydrogen chloride at this temperature for 5 hours. The mixture is cooled to room temperature and poured into 2.5 l of water. The mixture is neutralized to pH 7 with sodium hydroxide solution and the precipitated product is filtered off under suction. The material on the suction filter is taken up in methylene chloride, insoluble material is filtered off and the filtrate is washed with water, dried over magnesium sulphate and concentrated in half. By suction filtration and recrystallization from ethyl acetate there is obtained (S)-8-chloro-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carbothioamide of melting point 247°-248°.

後処理

  1. filtrationthe precipitated product is filtered off under suction
  2. filtrationThe material on the suction filter
  3. filtrationinsoluble material is filtered off
  4. washthe filtrate is washed with water
  5. dry with materialdried over magnesium sulphate
  6. concentrationconcentrated in half
  7. filtrationBy suction filtration and recrystallization from ethyl acetate

出典と根拠

ORDレコード
ord-010ef6def8a042bbb7fd7fb782719940
出典データセット
uspto-grants-1988_10
特許番号
US04775671

反応ノート

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