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Phenyl isocyanate → Tert-butyl 4-phenylcarbamoyl-1-piperazinecarboxylate

HRID 40577
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인쇄 미리보기

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HRID 40577 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[C:14]1([N:20]=[C:21]=[O:22])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>ClCCl>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:21](=[O:22])[NH:20][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7672Phenyl isocyanateHCID 143452tert-Butyl piperazine-1-carboxylate

생성물 1

HCID 20674603Tert-butyl 4-phenylcarbamoyl-1-piperazinecarboxylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of piperazine-1-carboxylic acid tert-butyl ester (114 g) in DCM (500 mL) was cooled in an ice bath and treated with phenyl isocyanate (65 mL). After 1 hour (h), the bath was removed. After 15 h, the resulting mixture was filtered and the solid was washed with dichloromethane (DCM, 2×100 mL), giving the title compound as a white amorphous solid (95 g).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customthe bath was removed
  • waitAfter 15 h
  • filtrationthe resulting mixture was filtered
  • washthe solid was washed with dichloromethane (DCM, 2×100 mL)
  • 출처 및 근거

    ORD 기록
    ord-fe996fa5dd974b17bd1c0e65a83a1254
    출처 데이터셋
    uspto-grants-2013_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08530476B2

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