ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Ici 109,081 → HCID 13193385、化合物

HRID 463657
ノート
印刷プレビュー

反応式

HRID 463657 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]([CH3:15])[CH2:10][C:11](=[O:14])[NH:12][N:13]=2)=[CH:4][CH:3]=1.[C:16]([C:18]([CH3:23])([CH3:22])[C:19](Cl)=[O:20])#[N:17]>N1C=CC=CC=1>[C:16]([C:18]([CH3:23])([CH3:22])[C:19]([NH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]([CH3:15])[CH2:10][C:11](=[O:14])[NH:12][N:13]=2)=[CH:4][CH:3]=1)=[O:20])#[N:17]
参加物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 161928Ici 109,081HCID 202649072-Cyano-2-methylpropanoyl chloride

生成物 1

HCID 13193385HCID 13193385、化合物収率 68.7%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

20.3 g (0.1 mole) of 6-(p-aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone were stirred with 15.8 g (0.12 mole) of 2-cyano-2-methylpropionyl chloride in 100 ml of pyridine for 3 hours at 0° C. 100 g of ice were added, after which the crystals were filtered off under suction, and the product was recrystallized from dimethylformamide/water and dried at 50° C. under greatly reduced pressure. 20.5 g (57%) of 6-[p-(2-cyano-2-methylpropionylamino)-phenyl]-4,5-dihydro-5-methyl-3(2H)-pyridazinone were obtained. Mp.: 225°-227° C.

後処理

  1. filtrationafter which the crystals were filtered off under suction
  2. customthe product was recrystallized from dimethylformamide/water
  3. customdried at 50° C. under greatly reduced pressure

出典と根拠

ORDレコード
ord-964ecc6452a244308ff1c25a998f7e7e
出典データセット
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04544562

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート