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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 1-(N-methyl-N-phenylaminocarbonyl)piperazine hydrochloride

HRID 22958
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인쇄 미리보기

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HRID 22958 반응식
C(#N)C.C(O[C:9]([N:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1)=[O:10])(C)(C)C.[CH3:17][N:18]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)C([Cl:21])=O.Cl>C(N(CC)CC)C>[ClH:21].[CH3:17][N:18]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:9]([N:11]1[CH2:12][CH2:13][NH:14][CH2:15][CH2:16]1)=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 6342AcetonitrileHCID 77969Carbamic chloride, N-methyl-N-phenyl-HCID 143452tert-Butyl piperazine-1-carboxylate

생성물 1

HCID 225913691-(N-methyl-N-phenylaminocarbonyl)piperazine hydrochloride

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

An acetonitrile (7 ml) solution containing N-(tert-butoxycarbonyl)piperazine (700 mg), N-methyl-N-phenylcarbamoyl chloride (700 mg) and triethylamine (1.05 mL) was stirred at room temperature for 15 hours to undergo reaction, and the resulting compound was acid-treated with hydrochloric acid to obtain 1-(N-methyl-N-phenylaminocarbonyl)piperazine.hydrochloride.

후처리

  1. customreaction

출처 및 근거

ORD 기록
ord-e805a6f4dfc941a1bf33986745408cfb
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06849622B2

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