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Rac-4-(2-amino-1-phenyl-ethyl)-1-benzyl-piperidine-4-carboxylic acid ethyl ester → Rac-8-benzyl-4-phenyl-2,8-diaza-spiro[4.5]decan-1-one

HRID 347303
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인쇄 미리보기

반응식

HRID 347303 반응식
C([O:3][C:4]([C:6]1([CH:19]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH2:20][NH2:21])[CH2:11][CH2:10][N:9]([CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:8][CH2:7]1)=O)C>C1(C)C=CC=CC=1>[CH2:12]([N:9]1[CH2:10][CH2:11][C:6]2([C:4](=[O:3])[NH:21][CH2:20][CH:19]2[C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH2:7][CH2:8]1)[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 66918079Rac-4-(2-amino-1-phenyl-ethyl)-1-benzyl-piperidine-4-carboxylic acid ethyl ester

생성물 1

HCID 21082592Rac-8-benzyl-4-phenyl-2,8-diaza-spiro[4.5]decan-1-one수율 58%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A solution of rac-4-(2-amino-1-phenyl-ethyl)-1-benzyl-piperidine-4-carboxylic acid ethyl ester (2.9 g, 8 mmol) in toluene (30 mL) was heated under reflux for 4 h. After cooling to room temperature and evaporation the mixture was purified by chromatography on silica gel eluting with DCM:MeOH:NH4OH (95:4.5:0.5) to afford the title compound (1.47 g, 58%) as a white solid. MS: m/e=321.4 (M+H).

후처리

  1. temperature
under reflux for 4 h
  • customevaporation the mixture
  • customwas purified by chromatography on silica gel eluting with DCM:MeOH:NH4OH (95:4.5:0.5)
  • 출처 및 근거

    ORD 기록
    ord-59b7bfbcd21a43e787c5dae10e6ef251
    출처 데이터셋
    uspto-grants-2007_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07173133B2

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