Water → 7-Chloro-5-methoxy-1-methyl-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one

HRID 441485노트

반응식

HRID 441485 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:11][C:10](=[O:12])[CH:9]=[N:8][C:7]([O:19][CH3:20])([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:6]=2[CH:21]=1.CI.O.[CH2:25](OCC)C>CN(C)C=O.[H-].[Na+]>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]([CH3:25])[C:10](=[O:12])[CH:9]=[N:8][C:7]([O:19][CH3:20])([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:6]=2[CH:21]=1

참가 물질

7

반응물 4

HCID 962WaterHCID 3283Diethyl EtherHCID 6328Methyl iodideHCID 30463447-Chloro-5-methoxy-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one

생성물 1

HCID 30467277-Chloro-5-methoxy-1-methyl-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 24758Sodium hydride용매

실험 절차

To a solution of 7-chloro-5-methoxy-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one (600 mg) in dry dimethylformamide (2 ml), sodium hydride (50% suspension in a mineral oil; 106 mg) is added under ice-cooling, and the resultant mixture is stirred at room temperature for 10 minutes. Methyl iodide (740 mg) is added to the mixture, which is stirred at room temperature for 5 minutes. The reaction mixtute is poured into icy water and shaken with diethyl ether. The organic layer is washed with water, dried over sodium sulfate, and evaporated to remove the solvent. The residue is crystallized from isopropyl ether to give 7-chloro-5-methoxy-1-methyl-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one (381 mg) as colorless prisms melting at 146.5 to 147° C.

후처리

  1. addition106 mg) is added under ice-
  2. temperaturecooling
  3. washThe organic layer is washed with water
  4. dry with materialdried over sodium sulfate
  5. customevaporated
  6. customto remove the solvent
  7. customThe residue is crystallized from isopropyl ether

출처 및 근거

ORD 기록
ord-e908a75da861462a9385108fbb0f61d5
출처 데이터셋
uspto-grants-1977_08
특허 번호
US04041026

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