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

Phosphorus oxychloride → HCID 58305987、化合物

HRID 2088687
ノート
印刷プレビュー

反応式

HRID 2088687 の反応式
P(Cl)(Cl)([Cl:3])=O.[CH2:6]([O:8][C:9](=[O:35])[CH2:10][N:11]1[CH2:16][CH2:15][CH:14]([C:17]2[N:25]=[C:24]3[N:19]([C:20](=O)[NH:21][C:22]([C:26]4[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:27]=4[Cl:33])=[CH:23]3)[N:18]=2)[CH2:13][CH2:12]1)[CH3:7]>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1>[CH2:6]([O:8][C:9](=[O:35])[CH2:10][N:11]1[CH2:12][CH2:13][CH:14]([C:17]2[N:25]=[C:24]3[N:19]([C:20]([Cl:3])=[N:21][C:22]([C:26]4[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:27]=4[Cl:33])=[CH:23]3)[N:18]=2)[CH2:15][CH2:16]1)[CH3:7]
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 24813Phosphorus oxychlorideHCID 136104186Ethyl {4-[7-(2,4-dichlorophenyl)-5-oxo-5,6-dihydro[1,2,4]triazolo[1,5-c]pyrimidin-2-yl]piperidin-1-yl}acetate

生成物 1

HCID 58305987HCID 58305987、化合物

試薬・触媒・溶媒 1

HCID 66133Benzyl triethylammonium chloride触媒

反応条件

温度
120 °C

実験手順

5 ml of phosphoryl chloride were added to 500 mg (1.11 mmol) of ethyl{4-[7-(2,4-dichlorophenyl)-5-oxo-5,6-dihydro [1,2,4]triazolo[1,5-c]-pyrimidin-2-yl]piperidin-1-yl}acetate (Example 54A), 1.01 g (4.44 mmol) of benzyltriethylammonium chloride were added and the reaction mixture was stirred at 120° C. for 2.5 h. The reaction mixture was concentrated and carefully, with vigorous stirring, added to saturated aqueous sodium bicarbonate solution. The pH was adjusted to pH=7 by addition of solid sodium bicarbonate. The aqueous phase was extracted three times with dichloromethane. The combined organic phases were washed once with water, dried with magnesium sulfate and then freed from the solvent. Without further purification, this gave 506 mg (88% of theory) of the product.

後処理

  1. additionwere added
  2. concentrationThe reaction mixture was concentrated
  3. additioncarefully, with vigorous stirring, added to saturated aqueous sodium bicarbonate solution
  4. additionThe pH was adjusted to pH=7 by addition of solid sodium bicarbonate
  5. extractionThe aqueous phase was extracted three times with dichloromethane
  6. washThe combined organic phases were washed once with water
  7. dry with materialdried with magnesium sulfate
  8. customWithout further purification

出典と根拠

ORDレコード
ord-ffdb0c00752c4fbeb20f7d1f543016be
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08436003B2

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