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

HRID 2289553
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HRID 2289553 반응식
Cl.C(OC([N:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:20]=[C:19]([Cl:21])[N:18]=[CH:17][N:16]=2)[CH2:11][CH2:10]1)=O)(C)(C)C>C(OCC)(=O)C>[ClH:21].[Cl:21][C:19]1[N:18]=[CH:17][N:16]=[C:15]([N:12]2[CH2:13][CH2:14][NH:9][CH2:10][CH2:11]2)[CH:20]=1
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 18697980tert-Butyl 4-(6-chloropyrimidin-4-yl)piperazine-1-carboxylate

생성물 1

HCID 186979794-Chloro-6-(piperazin-1-yl)pyrimidine hydrochloride수율 200.4%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매2회

실험 절차

Ethyl acetate saturated with gaseous HCl was added to a solution of 1-(tert-butoxycarbonyl)-4-(6-chloro-pyrimidin-4-yl)piperazine (16.80 g) in ethyl acetate (50 ml) and the resulting suspension stirred at ambient temperature for 3 hours. Solvent was evaporated to give (6-chloro-pyrimidin-4-yl)piperazine hydrochloride (13.25 g) as a cream solid.

후처리

  1. customSolvent was evaporated

출처 및 근거

ORD 기록
ord-43ece320d2f443b68284d114248a097a
출처 데이터셋
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06093718

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