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Hydrazine → HCID 68635306、化合物

HRID 1252369
ノート
印刷プレビュー

反応式

HRID 1252369 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 68635306HCID 68635306、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
-10 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-e55d63fd8a0148d7bf6d53f5d4c7355c
出典データセット
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04743586

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート