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2-Bromo-1-(thiophen-2-yl)ethan-1-one → HCID 12791243, 화합물

HRID 1906149
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인쇄 미리보기

반응식

HRID 1906149 반응식
Br.[Br:2][C:3]1[CH:4]=[N:5][C:6](=[O:9])[NH:7][CH:8]=1.Br[CH2:11][C:12]([C:14]1[S:15][CH:16]=[CH:17][CH:18]=1)=[O:13]>C(N(CC)CC)C.C(O)C>[Br:2][C:3]1[CH:4]=[N:5][C:6](=[O:9])[N:7]([CH2:11][C:12](=[O:13])[C:14]2[S:15][CH:16]=[CH:17][CH:18]=2)[CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 27763722-Bromo-1-(thiophen-2-yl)ethan-1-oneHCID 127955335-Bromopyrimidin-2(1H)-one hydrobromide

생성물 1

HCID 12791243HCID 12791243, 화합물

시약·촉매·용매 2

HCID 702Ethanol용매HCID 8471Triethylamine용매

실험 절차

A suspension of 5-bromopyrimidin-2-one hydrobromide (780 mg) and 2-bromoacetylthiophene (633 mg) in triethylamine (1 ml) and ethanol (20 ml) was stirred at ambient temperature for 11/2 hours. A solution formed within 10 minutes but a suspension subsequently resulted. This was chilled in ice, and the collected solid was crystallised from acetone to give the title pyrimidinone: yield 293 mg; m.p. 173°-175° C. dec; λmaxEtOH 259.5 nm (ε 9470), 287 nm (ε 6830), 332 nm (ε 2780).

후처리

  1. customA solution formed within 10 minutes
  2. customa suspension subsequently resulted
  3. temperatureThis was chilled in ice
  4. customthe collected solid was crystallised from acetone

출처 및 근거

ORD 기록
ord-b40156b582e4475e90be585199500c68
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04650800

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