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Piperazine → 4-Chloro-6-(piperazin-1-yl)pyrimidine hydrochloride

HRID 2376655
노트
인쇄 미리보기

반응식

HRID 2376655 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[CH:4][N:3]=1.[NH:9]1[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1>C(#N)C>[ClH:1].[Cl:8][C:6]1[N:5]=[CH:4][N:3]=[C:2]([N:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4837PiperazineHCID 709434,6-Dichloropyrimidine

생성물 1

HCID 186979794-Chloro-6-(piperazin-1-yl)pyrimidine hydrochloride

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

반응 조건

온도
2.5 °C

실험 절차

A solution of 14.8 g of 4,6-dichloropyrimidine in 100 ml of acetonitrile is cooled to 0-5° C., a solution of 20 g of anhydrous piperazine in 200 ml of acetonitrile is added over 30 minutes and the mixture is left with stirring at 0-5° C. for 2 hours. It is concentrated under vacuum, the residue is taken up with 100 ml of 2N NaOH and extracted with ether, the organic phase is dried over Na2SO4 and the solvent is evaporated under vacuum. The hydrochloride is formed, giving 15 g of the expected product.

후처리

  1. waitthe mixture is left
  2. concentrationIt is concentrated under vacuum
  3. extractionextracted with ether
  4. dry with materialthe organic phase is dried over Na2SO4
  5. customthe solvent is evaporated under vacuum

출처 및 근거

ORD 기록
ord-f6a0cefb2a014cd68ce8c899835c8e0d
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07468368B2

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