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Morpholine → 4-(2-Chloroquinazolin-4-yl)morpholine

HRID 2071757
ノート
印刷プレビュー

反応式

HRID 2071757 の反応式
[Cl:1][C:2]1[N:11]=[C:10](Cl)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[NH:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1>C(O)C.O>[Cl:1][C:2]1[N:11]=[C:10]([N:13]2[CH2:18][CH2:17][O:16][CH2:15][CH2:14]2)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 8083MorpholineHCID 2528862,4-Dichloroquinazoline2 回

生成物 1

HCID 23384664-(2-Chloroquinazolin-4-yl)morpholine収率 73.7%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

Twenty grams of 2,4-dichloroquinazoline was suspended in 200 ml of ethanol. To this suspension was added 17.4 g of morpholine. A mildly exothermic reaction ensued with the concomitant dissolution of the suspended dichloroquinazoline. When the reaction subsided, after about 10 minutes, the mixture was heated at reflux for 15 minutes, and then was allowed to cool. The reaction mixture then was diluted with 800 ml of water. The solid which precipitated was collected by filtration and was washed with water. After drying, the solid was recrystallized from 1:2 benzene-hexane, to give 18.5 g of 2-chloro-4-morpholinoquinazoline; m.p. 103°-105°. The following analytical data were obtained:

後処理

  1. customA mildly exothermic reaction
  2. temperaturethe mixture was heated
  3. temperatureat reflux for 15 minutes
  4. temperatureto cool
  5. customThe solid which precipitated
  6. filtrationwas collected by filtration
  7. washwas washed with water
  8. customAfter drying
  9. customthe solid was recrystallized from 1:2 benzene-hexane

出典と根拠

ORDレコード
ord-61b4bf8b75694a07bda18beebb21ff0f
出典データセット
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04048312

反応ノート

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