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2-Bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethan-1-one → HCID 21258525, 화합물

HRID 635345
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HRID 635345 반응식
[Br:1][CH2:2][C:3]([C:5]1([C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[C:11]([Cl:16])[CH:10]=2)[CH2:8][CH2:7][CH2:6]1)=[O:4].[N:17]1[CH2:22][CH2:21][CH2:20][NH:19][C:18]=1[SH:23]>CC(C)=O>[BrH:1].[Cl:16][C:11]1[CH:10]=[C:9]([C:5]2([C:3](=[O:4])[CH2:2][S:23][C:18]3[NH:19][CH2:20][CH2:21][CH2:22][N:17]=3)[CH2:8][CH2:7][CH2:6]2)[CH:14]=[CH:13][C:12]=1[Cl:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 212584722-Bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethan-1-oneHCID 178527864HCID 178527864, 화합물

생성물 1

HCID 21258525HCID 21258525, 화합물수율 89.6%

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

A solution of 2-bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethanone (3.2 g) in acetone (25 ml) was added to a solution of 3,4,5,6-tetrahydropyrimidine-2-thiol (1.2 g) in acetone (150 mL), then the mixture was heated under reflux for 0.5 hour, and allowed to cool to ambient temperature. The resulting solid was collected by filtration and dried in vacuo at ambient temperature to give 1-[1-(3,4-dichlorophenyl)cyclobutyl]-2-(3,4,5,6-tetrahydropyrimidin-2-ylthio)ethanone hydrobromide as a white solid (3.9 g), m.p. 203-204° C.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 0.5 hour
  3. filtrationThe resulting solid was collected by filtration
  4. customdried in vacuo at ambient temperature

출처 및 근거

ORD 기록
ord-1e775baddea64a48be3bf2ee0ff36bc9
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06187802B1

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