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

HRID 1755859
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인쇄 미리보기

반응식

HRID 1755859 반응식
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]
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참가 물질

4

반응물 2

HCID 218054064-(4-Chloro-5-pyrimidinyl)-o-phenylene diacetateHCID 53442613Sodium hydrogen sulfide hydrate

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
60 °C

실험 절차

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.).

후처리

  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

출처 및 근거

ORD 기록
ord-f181397c4013493983b720e1d437bd57
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05438052

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