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Phosphorus oxychloride → 4-Chloro-5-(2,6-dichloroanilinomethyl)-2-methylthiopyrimidine

HRID 1858315
ノート
印刷プレビュー

反応式

HRID 1858315 の反応式
[Cl:1][C:2]1[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[C:3]=1[NH:4][CH2:5][C:6]1[C:7](=O)[NH:8][C:9]([S:12][CH3:13])=[N:10][CH:11]=1.P(Cl)(Cl)([Cl:22])=O>>[Cl:22][C:7]1[C:6]([CH2:5][NH:4][C:3]2[C:2]([Cl:1])=[CH:18][CH:17]=[CH:16][C:15]=2[Cl:19])=[CH:11][N:10]=[C:9]([S:12][CH3:13])[N:8]=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 22125077HCID 22125077、化合物

生成物 1

HCID 221250524-Chloro-5-(2,6-dichloroanilinomethyl)-2-methylthiopyrimidine収率 22%

反応条件

温度
100 °C

実験手順

13.6 g (43 mmol) of crude 5-(2,6-dichloroanilinomethyl)-2-methylthio-3H-pyrimidin-4-one was treated with 120 ml of phosphorus oxychloride and the mixture heated at 100° C. for 15 minutes then cooled. The mixture was evaporated and cautiously partitioned between 200 ml of ethyl acetate and 200 ml of water. The organic phase was dried over magnesium sulfate, filtered and evaporated. The product was purified by flash chromatography on silica gel eluting with diethyl ether/isohexane in a ratio of 1:9 to give 3.2 g (22%) of 4-chloro-5-(2,6-dichloroanilinomethyl)-2-methylthiopyrimidine as a pale yellow oil. [Mass spectrum (ESI) MH+ =334].

後処理

  1. temperaturethen cooled
  2. customThe mixture was evaporated
  3. customcautiously partitioned between 200 ml of ethyl acetate and 200 ml of water
  4. dry with materialThe organic phase was dried over magnesium sulfate
  5. filtrationfiltered
  6. customevaporated
  7. customThe product was purified by flash chromatography on silica gel eluting with diethyl ether/isohexane in a ratio of 1:9

出典と根拠

ORDレコード
ord-c8f7a8a58f324eb3902d911e187dfab3
出典データセット
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06150373

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