반응 #1168

ord-a6aacc5162fa4403a0432cd2a4af49bf

반응 방정식

CC(=O)C(C#N)c1ccc(NC(=O)OC(C)(C)C)cc1
2-(4-t-butoxycarbonylaminophenyl)-3-oxobutyronitrile
CCO
ethanol
CCOC(CNN)OCC
2,2-diethoxyethylhydrazine
Cl
hydrogen chloride
Cc1nn2cc[nH]c2c1-c1ccc(N)cc1.Cl
title compound
Cc1nn2cc[nH]c2c1-c1ccc(N)cc1.Cl
7-(4-Aminophenyl)-6-methyl-1H-imidazo[1,2-b]-pyrazole hydrochloride

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도under reflux for 2 hours
  3. 3
    온도the whole mixture was heated
  4. 4
    온도under reflux for a further 30 minutes
  5. 5
    온도After the mixture had been cooled
  6. 6
    기타to precipitate crystals
  7. 7
    여과These crystals were collected by filtration
  8. 8
    기타recrystallized from ethanol

실험 절차

A mixture of 2.5 g of 2-(4-t-butoxycarbonylaminophenyl)-3-oxobutyronitrile, 20 ml of ethanol and 1.4 g of 2,2-diethoxyethylhydrazine was heated under reflux for 2 hours. 20 ml of 4N hydrogen chloride in dioxane were added, and then the whole mixture was heated under reflux for a further 30 minutes. After the mixture had been cooled, ethyl acetate was added to precipitate crystals. These crystals were collected by filtration and recrystallized from ethanol to give 1.4 g of the title compound as pale brown plates melting at 180°-190° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723481uspto-grants-1998_03