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1-Benzyl-4-(2-methylphenyl)piperazine-2-carboxamide → 2-Carbamoyl-4-(2-methylphenyl)piperazine

HRID 128579
노트
인쇄 미리보기

반응식

HRID 128579 반응식
C([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[CH3:20])[CH2:10][CH:9]1[C:21]([NH2:23])=[O:22])C1C=CC=CC=1.[H][H]>CO.C(O)C.[OH-].[OH-].[Pd+2]>[CH3:20][C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=1[N:11]1[CH2:12][CH2:13][NH:8][CH:9]([C:21]([NH2:23])=[O:22])[CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 218372261-Benzyl-4-(2-methylphenyl)piperazine-2-carboxamideHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 154305682-Carbamoyl-4-(2-methylphenyl)piperazine

시약·촉매·용매 3

HCID 9942167Palladium hydroxide촉매HCID 702Ethanol용매HCID 887Methanol용매

실험 절차

1-benzyl-4-(2-methylphenyl)piperazine-2-carboxamide (2.64 g, 8.53 mmol) and palladium hydroxide/carbon (430 mg) were combined in a mixture of methanol (35 ml) and ethanol (35 ml) and shaken in an atmosphere of hydrogen at 55 psi for 6 hours at ambient temperature. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was reconcentrated in vacuo from ether three times to provide 4-(2-methylphenyl)piperazine-2-carboxamide.

후처리

  1. filtrationThe mixture was filtered
  2. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-53ec8bbd7bab469b8220dbfaecb12282
출처 데이터셋
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05464788

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