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Ethanolamine → HCID 22918635, 화합물

HRID 1376888
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HRID 1376888 반응식
[CH2:1]([N:8]1[C:12](Br)=[C:11]([N+:14]([O-:16])=[O:15])[C:10]([Br:17])=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.[CH2:19]([CH2:21][NH2:22])[OH:20]>>[CH2:1]([N:8]1[C:12]([NH:22][CH2:21][CH2:19][OH:20])=[C:11]([N+:14]([O-:16])=[O:15])[C:10]([Br:17])=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 700EthanolamineHCID 962WaterHCID 196972381-benzyl-3,5-dibromo-4-nitro-1H-pyrazole

생성물 1

HCID 22918635HCID 22918635, 화합물

실험 절차

3.61 (10 mmoles) of 1-benzyl-3,5-dibromo-4-nitropyrazole are heated at 80° C. in 15 ml ethanolamine for 2 hours. After cooling, the reaction mixture is poured on 30 ml water and the separated precipitate is collected by filtration. After recrystallizing once from toluene, 2.5 g (74 percent of theory) of 1-benzyl-3-bromo-5-(2'-hydroxyethyl)amino-4-nitropyrazole are obtained in the form of pale yellow crystals with a melting point of 110° to 112° C.

후처리

  1. temperatureAfter cooling
  2. filtrationthe separated precipitate is collected by filtration
  3. custom
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
After recrystallizing once from toluene, 2.5 g (74 percent of theory) of 1-benzyl-3-bromo-5-(2'-hydroxyethyl)amino-4-nitropyrazole
  • customare obtained in the form of pale yellow crystals with a melting point of 110° to 112° C.
  • 출처 및 근거

    ORD 기록
    ord-f3d0a10462fe43528a121baef4c9152c
    출처 데이터셋
    uspto-grants-1997_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05663366

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