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

Acetyl chloride → N-(4,6-Dichloropyrimidin-2-yl)acetamide

HRID 1730144
ノート
印刷プレビュー

反応式

HRID 1730144 の反応式
C(O[C:5](=[O:7])[CH3:6])(=O)C.[NH2:8][C:9]1[N:14]=[C:13]([Cl:15])[CH:12]=[C:11]([Cl:16])[N:10]=1.C(Cl)(=O)C>>[C:5]([NH:8][C:9]1[N:14]=[C:13]([Cl:15])[CH:12]=[C:11]([Cl:16])[N:10]=1)(=[O:7])[CH3:6]
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 3

HCID 6367Acetyl chlorideHCID 7918Acetic AnhydrideHCID 655222-Amino-4,6-dichloropyrimidine

生成物 1

HCID 12611964N-(4,6-Dichloropyrimidin-2-yl)acetamide

反応条件

温度
110 °C

実験手順

A 250 ml. three necked flask was fitted with a mechanical stirrer and a reflux condenser with drying tube. The flask is charged with 50 ml. of acetic anhydride and 3.85 g of 2-amino-4,6-dichloropyrimidine (0.025 mole). Then, 10 ml. of acetyl chloride was added slowly and the mixture was heated to 110° C for 8 hours. The mixture was allowed to stand overnight at room temperature. The crystalline solid product which formed was filtered and washed with water and sodium bicarbonate solution. It was then recrystallized from 50% alcohol. There was obtained 3.8 g of 2-acetamido-4,6-dichloropyrimidine (PY-25) in the form of white crystals, melting point, 198°-200° C, yield, 74.5%.

後処理

  1. customthree necked flask was fitted with a mechanical stirrer and a reflux condenser
  2. customwith drying tube
  3. additionThe flask is charged with 50 ml
  4. customThe crystalline solid product which formed
  5. filtrationwas filtered
  6. washwashed with water and sodium bicarbonate solution
  7. customIt was then recrystallized from 50% alcohol

出典と根拠

ORDレコード
ord-d9a1175b5f344b87b702f550625511ad
出典データセット
uspto-grants-1976_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03991190

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