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Sodium Hydroxide → 3-chloro-N-[3-(1H-imidazol-1-yl)propyl]benzamide

HRID 1589174
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HRID 1589174 반응식
Cl.Cl.[N:3]1([CH2:8][CH2:9][CH2:10][NH2:11])[CH:7]=[CH:6][N:5]=[CH:4]1.[OH-].[Na+].[Cl:14][C:15]1[CH:16]=[C:17]([CH:21]=[CH:22][CH:23]=1)[C:18](Cl)=[O:19]>C(Cl)Cl>[Cl:14][C:15]1[CH:16]=[C:17]([CH:21]=[CH:22][CH:23]=1)[C:18]([NH:11][CH2:10][CH2:9][CH2:8][N:3]1[CH:7]=[CH:6][N:5]=[CH:4]1)=[O:19]
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참가 물질

5

반응물 3

HCID 14798Sodium Hydroxide2회HCID 69252Benzoyl chloride, 3-chloro-HCID 122509693-(Imidazole-1-yl)-propylamine Dihydrochloride

생성물 1

HCID 28482203-chloro-N-[3-(1H-imidazol-1-yl)propyl]benzamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A mixture of 6.0 g. of 1H-imidazole-1-propanamine dihydrochloride, 45 ml. of 2N sodium hydroxide and 150 ml. of methylene chloride was stirred at room temperature and 3.9 ml. of 3-chlorobenzoyl chloride was added. The reaction mixture was stirred for 18 hours, then methylene chloride and 15 ml. of 1N sodium hydroxide were added and the layers were separated. The organic layer was washed with water, dried over magnesium sulfate, and concentrated to remove the solvent. The residue was triturated with diethyl ether and the crystalline product recovered by filtration and recrystallized from ethanol, giving the desired product, m.p. 125°-127° C.

후처리

  1. additionA mixture of 6.0 g
  2. customthe layers were separated
  3. washThe organic layer was washed with water
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customto remove the solvent
  7. customThe residue was triturated with diethyl ether
  8. filtrationthe crystalline product recovered by filtration
  9. customrecrystallized from ethanol

출처 및 근거

ORD 기록
ord-e7a99a1e55744f3d8b8b83b92d1c4af8
출처 데이터셋
uspto-grants-1986_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04568687

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