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Hydrazine → HCID 68635306, 화합물

HRID 1252369
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HRID 1252369 반응식
[CH3:1][C:2]1[NH:6][C:5]([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=2)=[N:4][C:3]=1[C:13]([O:15]CC)=O.[NH2:18][NH2:19]>C(O)C>[CH3:1][C:2]1[NH:6][C:5]([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=2)=[N:4][C:3]=1[C:13]([NH:18][NH2:19])=[O:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9321HydrazineHCID 534358745-Methyl-2-pyridin-3-YL-3H-imidazole-4-carboxylic acid ethyl ester

생성물 1

HCID 68635306HCID 68635306, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
-10 °C

실험 절차

A solution of 32 g of 5-methyl-2-(3-pyridinyl)-1H-imidazole-4-carboxylic acid, ethyl ester (prepared as described above) in ethanol was heated to boiling. A 79 ml portion of hydrazine was added. This mixture was stirred at reflux for 14 hours and then cooled to -10° C. The mixture was taken to dryness in vacuo and then evaporated to dryness in vacuo twice from 125 ml portions of methyl cellosolve. The residue was shaken with 100 ml of ethanol and the solids collected, washed with 100 ml of ethanol and two 100 ml portions of ether and dried at 60° C. in vacuo, giving 18.7 g of 5-methyl-2-(3-pyridinyl)-1H-imidazole-4-carboxylic acid, hydrazide.

후처리

  1. temperatureat reflux for 14 hours
  2. customevaporated to dryness in vacuo twice from 125 ml portions of methyl cellosolve
  3. stirringThe residue was shaken with 100 ml of ethanol
  4. customthe solids collected
  5. washwashed with 100 ml of ethanol and two 100 ml portions of ether
  6. customdried at 60° C. in vacuo

출처 및 근거

ORD 기록
ord-e55d63fd8a0148d7bf6d53f5d4c7355c
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04743586

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