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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Bromine → 1-(5-Bromopyrimidin-2-yl)piperazine

HRID 364621
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HRID 364621 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[N:7]1[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]1.[Br:13]Br>Cl>[Br:13][C:5]1[CH:6]=[N:1][C:2]([N:7]2[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]2)=[N:3][CH:4]=1
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참가 물질

4

반응물 2

HCID 24408BromineHCID 887471-(2-Pyrimidinyl)piperazine

생성물 1

HCID 27571751-(5-Bromopyrimidin-2-yl)piperazine수율 62%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

This example serves to illustrate procedure B of Scheme 2. To an ice-cooled solution of 1-(2-pyrimidinyl)piperazine (16.4 g, 0.1 mole) in 1N HCl (100 mL) was added dropwise bromine (15.98 g, 0.1 mole). After stirring at 0° for 0.5 hr, the mixture was heated to 100° until dissipation of the red color had occurred. The mixture is filtered, cooled, made alkaline with 50% NaOH and extracted with ether. The dried extract (MgSO4) was concentrated in vacuo to provide 14.5 g (62%) of product, m.p. 73°-75°.

후처리

  1. temperaturethe mixture was heated to 100° until dissipation of the red color
  2. filtrationThe mixture is filtered
  3. temperaturecooled
  4. extractionextracted with ether
  5. extractionThe dried extract (MgSO4)
  6. concentrationwas concentrated in vacuo

출처 및 근거

ORD 기록
ord-c3ca85b0010e449b8758d7dfd7ba1914
출처 데이터셋
uspto-grants-1986_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04605655

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