Isopropanol → Diazepam

HRID 262941

반응식

HRID 262941 반응식
Br[CH2:2][C:3]([N:5]([C:7]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:8]=1[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=O)[CH3:6])=[O:4].C1N2CN3CN(C2)C[N:23]1C3.[Br-].[NH4+].C(O)(C)C>O>[Cl:21][C:18]1[CH:19]=[CH:20][C:7]2[N:5]([CH3:6])[C:3](=[O:4])[CH2:2][N:23]=[C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:8]=2[CH:17]=1

참가 물질

6

반응물 4

HCID 3776IsopropanolHCID 4101HexamethylenetetramineHCID 25514Ammonium BromideHCID 76099N-(2-benzoyl-4-chlorophenyl)-2-bromo-N-methylacetamide

생성물 1

HCID 3016Diazepam

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Reflux 1.8 g. (0.005 moles) of 2-(2-bromo-N-methylacetamido)-5-chlorobenzophenone, 2.8 g. (0.020 moles) of hexamethylenetetramine and 1.96 g. (0.020 moles) of ammonium bromide together for 2 hours in 14 ml. of 85% (v/v) aqueous isopropyl alcohol. Pour the reaction mixture into water and extract the product with benzene. Wash the benzene solution with water, dry over anhydrous sodium sulfate, filter and evaporate to dryness. After recrystallization, 7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one is obtained. The material gives a single spot by thin layer chromatography, and after drying under vacuum at 110° C., shows no depression on mixed melting point with an authentic sample (M.P. 129.5°-130.5° C.).

후처리

  1. temperatureReflux 1.8 g
  2. extractionextract the product with benzene
  3. washWash the benzene solution with water
  4. dry with materialdry over anhydrous sodium sulfate
  5. filtrationfilter
  6. customevaporate to dryness
  7. customAfter recrystallization

출처 및 근거

ORD 기록
ord-6b061085fce449f7b748aa91c5b9620d
출처 데이터셋
uspto-grants-1979_05
특허 번호
US04155904

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