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Methylhydrazine → HCID 178481737、化合物

HRID 1748821
ノート
印刷プレビュー

反応式

HRID 1748821 の反応式
O=[C:2]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)[CH2:3][C:4](OCC)=[O:5].[CH3:15][NH:16][NH2:17]>CCO>[CH3:15][N:16]1[C:4]([OH:5])=[CH:3][C:2]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=2)=[N:17]1
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 6061MethylhydrazineHCID 2736461Ethyl 3-oxo-3-(pyridin-2-yl)propanoate

生成物 1

HCID 178481737HCID 178481737、化合物収率 79%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
85 °C

実験手順

To a solution of ethyl 3-oxo-3-(pyridin-2-yl)propanoate (25.00 g, 129 mmol, Matrix Scientific) in EtOH (60 mL) was added methylhydrazine (6.81 mL, 129 mmol). The mixture was heated at about 85° C. for about 3 h then cooled to rt and concentrated at rt under reduced pressure. The material was triturated with Et2O (40 mL). The solids were collected by filtration then washed with Et2O to give 1-methyl-3-(pyridin-2-yl)-1H-pyrazol-5-ol (17.80 g, 79%). The filtrate was concentrated under reduced pressure then the material was triturated with 1:1 DCM/Et2O. The solids were collected by filtration and washed with Et2O to give a second crop of 1-methyl-3-(pyridin-2-yl)-1H-pyrazol-5-ol (1.20 g, 5%): LC-MS (Table 1, Method g) Rt=1.05 min, m/z 176 (M+H)+; 1H-NMR (DMSO, Bruker 400 MHz) δ 11.05 (s, 1H), 8.50-8.47 (m, 1H), 7.83-7.80 (m, 1H), 7.78-7.69 (m, 1H), 7.24-7.19 (m, 1H), 5.90 (s, 1H), 3.57 (s, 3H).

後処理

  1. temperaturethen cooled to rt
  2. concentrationconcentrated at rt under reduced pressure
  3. customThe material was triturated with Et2O (40 mL)
  4. filtrationThe solids were collected by filtration
  5. washthen washed with Et2O

出典と根拠

ORDレコード
ord-4274f93feedb4eafb66e06158be77451
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09150592B2

反応ノート

読み込み中…

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