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Methylamine → HCID 22918634, 화합물

HRID 1376886
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HRID 1376886 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.[CH3:18][NH2:19]>O>[CH2:1]([N:8]1[C:12]([NH:19][CH3:18])=[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 2

HCID 6329MethylamineHCID 196972381-benzyl-3,5-dibromo-4-nitro-1H-pyrazole

생성물 1

HCID 22918634HCID 22918634, 화합물수율 87%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

3.61 g (10 mmoles) of 1-benzyl -3,5-dibromo-4-nitropyrazole are heated in 100 ml of a 35-percent solution of methylamine in water for 4 hours at 60° C. After cooling, the separated precipitate is collected by filtration and recrystallized once from ethanol. 2.7 g (87 percent of theory) of 1-benzyl-3-bromo-5-methylamino-4-nitropyrazole are obtained in the form of colorless crystals with a melting point of 116° C.

후처리

  1. temperatureAfter cooling
  2. filtrationthe separated precipitate is collected by filtration
  3. customrecrystallized once from ethanol

출처 및 근거

ORD 기록
ord-247c1dad6cd749e790798edac8c27bb3
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05663366

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