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4-(4-Chloro-5-pyrimidinyl)-o-phenylene diacetate → 5-(3,4-dihydroxyphenyl)-4(3H)-pyrimidinethione

HRID 1755859
ノート
印刷プレビュー

反応式

HRID 1755859 の反応式
C([O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[C:12](Cl)=[N:13][CH:14]=[N:15][CH:16]=2)=[CH:7][C:6]=1[O:18]C(=O)C)(=O)C.O.[SH2:23].[Na]>CO>[OH:18][C:6]1[CH:7]=[C:8]([C:11]2[C:12](=[S:23])[NH:13][CH:14]=[N:15][CH:16]=2)[CH:9]=[CH:10][C:5]=1[OH:4]
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 218054064-(4-Chloro-5-pyrimidinyl)-o-phenylene diacetateHCID 53442613Sodium hydrogen sulfide hydrate

生成物 1

HCID 199178705-(3,4-dihydroxyphenyl)-4(3H)-pyrimidinethione収率 97.1%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
60 °C

実験手順

4-(4-Chloro-5-pyrimidinyl)-o-phenylene diacetate (1.1 g) (3.6 mmol) are dissolved in 30 ml of methanol. 1.56 g of sodium hydrogen sulphide hydrate are added thereto and the mixture is stirred at 60° C. for 4.5 hours. The solvent is distilled off in a vacuum and the residue is dissolved in 20 ml of water. The solution is acidified with dilute aqueous hydrochloric acid to pH 5, the precipitated product is filtered off under suction and washed with water and diethyl ether. After drying in a high vacuum there are obtained 770 mg of 5-(3,4-dihydroxyphenyl)-4(3H)-pyrimidinethione as yellow crystals of m.p. 235° C. (dec.).

後処理

  1. distillationThe solvent is distilled off in a vacuum
  2. dissolutionthe residue is dissolved in 20 ml of water
  3. filtrationthe precipitated product is filtered off under suction
  4. washwashed with water and diethyl ether
  5. customAfter drying in a high vacuum

出典と根拠

ORDレコード
ord-f181397c4013493983b720e1d437bd57
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05438052

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