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Phosphorus oxychloride → 5,6-Dimethyl-2-(4-methylthiazol-2-yl)amino-4-chloropyrimidine

HRID 275926
ノート
印刷プレビュー

反応式

HRID 275926 の反応式
[CH3:1][C:2]1[C:3](O)=[N:4][C:5]([NH:9][C:10]2[S:11][CH:12]=[C:13]([CH3:15])[N:14]=2)=[N:6][C:7]=1[CH3:8].P(Cl)(Cl)([Cl:19])=O>CN(C)C=O>[CH3:1][C:2]1[C:3]([Cl:19])=[N:4][C:5]([NH:9][C:10]2[S:11][CH:12]=[C:13]([CH3:15])[N:14]=2)=[N:6][C:7]=1[CH3:8]
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 24813Phosphorus oxychlorideHCID 178431960HCID 178431960、化合物

生成物 1

HCID 183156855,6-Dimethyl-2-(4-methylthiazol-2-yl)amino-4-chloropyrimidine収率 33.9%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

The mixture solution of 5,6-dimethyl-2-(4-methylthiazol-2-yl)amino-4-hydroxypyrimidine (1.15 g, 4-78 mmol), phosphorus oxychioride(7 ml), and dimethylformamide(5 ml) was heated to 70° C. for 30 minutes, cooled to a room temperature and then poured into ice water. The aqueous layer was extracted with dichloromethane, washed with 1N sodium hydroxide solution, and then washed with water. The separated organic layer was concentrated and the residual oil was suspended in a mixture solution of ethyl ether and hexane. The resulting solid was filtered and dried to give 0.42 g of the titled compound. (Yield: 33.9%)

後処理

  1. extractionThe aqueous layer was extracted with dichloromethane
  2. washwashed with 1N sodium hydroxide solution
  3. washwashed with water
  4. concentrationThe separated organic layer was concentrated
  5. filtrationThe resulting solid was filtered
  6. customdried

出典と根拠

ORDレコード
ord-8d5b275a824a498cbd117255cac1bb98
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06352993B1

反応ノート

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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