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Phosphorus oxychloride → 3-(6-Chloro-1,6-dihydro-pyridazin-4-yl)-N-methyl-benzamide

HRID 1097318
ノート
印刷プレビュー

反応式

HRID 1097318 の反応式
[CH3:1][NH:2][C:3](=[O:17])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]2[CH:11]=[N:12][NH:13][C:14](=O)[CH:15]=2)[CH:5]=1.O=P(Cl)(Cl)[Cl:20]>>[Cl:20][CH:14]1[NH:13][N:12]=[CH:11][C:10]([C:6]2[CH:5]=[C:4]([CH:9]=[CH:8][CH:7]=2)[C:3]([NH:2][CH3:1])=[O:17])=[CH:15]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

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 59443494N-Methyl-3-(6-oxo-1,6-dihydro-pyridazin-4-yl)-benzamide

生成物 1

HCID 594434963-(6-Chloro-1,6-dihydro-pyridazin-4-yl)-N-methyl-benzamide

反応条件

温度
110 °C

実験手順

N-Methyl-3-(6-oxo-1,6-dihydro-pyridazin-4-yl)-benzamide (1 eq, 3.14 mmol, 720 mg) is suspended in POCl3 (10 ml) and the reaction mixture is heated at 110° C. for 2 h. After cooling to room temperature, the solvent is removed in vacuo and then ice water is added. The pH is adjusted to pH8 with portionwise addition of sat. aqueous Na2CO3. The aqueous layer is extracted with EtOAc and the combined organic layers are washed with brine, dried over MgSO4, filtered and evaporated to dryness to yield 3-(6-Chloro-1,6-dihydro-pyridazin-4-yl)-N-methyl-benzamide as a yellow solid which did not require further purification; [M+H]+=248

後処理

  1. temperatureAfter cooling to room temperature
  2. customthe solvent is removed in vacuo
  3. additionice water is added
  4. additionThe pH is adjusted to pH8 with portionwise addition of sat. aqueous Na2CO3
  5. extractionThe aqueous layer is extracted with EtOAc
  6. washthe combined organic layers are washed with brine
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. customevaporated to dryness

出典と根拠

ORDレコード
ord-0f611b17aaa44e1a9c985430d4cc18b3
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08143253B2

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