Potassium Chloride → 1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thione

HRID 54964ノート

反応式

HRID 54964 の反応式
Cl.Cl.[CH3:3][NH:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[NH2:13].C([O-])(=O)C.[K+].[C:25](=S)=[S:26].C(S)(=S)N.[Cl-].[K+]>C(O)(C)C>[CH3:3][N:4]1[C:25](=[S:26])[NH:13][CH:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[CH2:5]1

参加物

7

実験手順

To a suspension of 15 g (50 mmol) of 2-[(methylamino)methyl]-α-phenylbenzenemethanamine dihydrochoride in 100 mL of isopropyl alcohol was added 10 g (100 mmol) of potassium acetate followed by 3.3 mL (55 mmol) of carbon disulfide in 35 mL of isopropyl alcohol. The suspension was stirred at room temperature for one and one-half hours and then refluxed for 30 minutes. The reaction was chilled in ice and the internal salt of the carbamodithioic acid, contaminated with two equivalents of of potassium chloride, was filtered off. The carbamodithioic acid was suspended in 125 mL of 95% ethanol, and 1.3 mL of of 12N hydrochloric acid was added. The suspension was refluxed for three days, cooled, and 15.3 g (114%) of the crude benzodiazepin-3-thione was filtered off. A 6-g portion of the crude product was recrystallized from 2-ethoxy ethanol to yield 2.0 g (38%) of product, mp 208-209.

後処理

  1. temperaturerefluxed for 30 minutes
  2. temperatureThe reaction was chilled in ice
  3. filtrationwas filtered off
  4. addition1.3 mL of of 12N hydrochloric acid was added
  5. temperatureThe suspension was refluxed for three days
  6. temperaturecooled
  7. filtration15.3 g (114%) of the crude benzodiazepin-3-thione was filtered off
  8. customA 6-g portion of the crude product was recrystallized from 2-ethoxy ethanol

出典と根拠

ORDレコード
ord-2068da37eed34df5b6bdbddc2bfafcbc
出典データセット
uspto-grants-1997_04
特許番号
US05624922

反応ノート

読み込み中…