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Sodium Methoxide → N-[3-(5-amino-1-methylpyrazol-4-yl)propyl]formamide

HRID 349524
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HRID 349524 반응식
Cl.Cl.[NH2:3][C:4]1[N:8]([CH3:9])[N:7]=[CH:6][C:5]=1[CH2:10][CH2:11][CH2:12][NH2:13].[CH3:14][O-:15].[Na+]>CO>[NH2:3][C:4]1[N:8]([CH3:9])[N:7]=[CH:6][C:5]=1[CH2:10][CH2:11][CH2:12][NH:13][CH:14]=[O:15]
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참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 179620333-(5-Amino-1-methylpyrazol-4-yl)propylamine dihydrochloride

생성물 1

HCID 17962035N-[3-(5-amino-1-methylpyrazol-4-yl)propyl]formamide

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a solution of 3-(5-amino-1-methylpyrazol-4-yl)propylamine dihydrochloride (9.3 g, 40 mmol) in methanol (80 ml) was added 28% sodium methoxide solution in methanol (15.9 g). The mixture was filtered through Celite, and the filtrate was concentrated in vacuo. A solution of the oily residue in ethyl formate (60 g) was stirred under reflux for 20 hours. After cooling, to the reaction mixture was added chloroform. The mixture was filtered through Celite, and the filtrate was concentrated in vacuo. The residue was triturated with ethyl acetate and dried in vacuo to give N-[3-(5-amino-1-methylpyrazol-4-yl)propyl]formamide (6.7 g) as a solid.

후처리

  1. filtrationThe mixture was filtered through Celite
  2. concentrationthe filtrate was concentrated in vacuo
  3. temperatureunder reflux for 20 hours
  4. temperatureAfter cooling, to the reaction mixture
  5. additionwas added chloroform
  6. filtrationThe mixture was filtered through Celite
  7. concentrationthe filtrate was concentrated in vacuo
  8. customThe residue was triturated with ethyl acetate
  9. customdried in vacuo

출처 및 근거

ORD 기록
ord-b3c889fb70a4440abb23ef21c5cfa33c
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07179801B2

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