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Rac-8-benzyl-4-phenyl-2,8-diaza-spiro[4.5]decan-1-one → 4-Phenyl-2,8-diazaspiro[4.5]decan-1-one

HRID 347304
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HRID 347304 반응식
C([N:8]1[CH2:24][CH2:23][C:11]2([C:15](=[O:16])[NH:14][CH2:13][CH:12]2[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH2:10][CH2:9]1)C1C=CC=CC=1>[Pd].C(Cl)Cl>[C:17]1([CH:12]2[C:11]3([CH2:10][CH2:9][NH:8][CH2:24][CH2:23]3)[C:15](=[O:16])[NH:14][CH2:13]2)[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

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

생성물 1

HCID 127097244-Phenyl-2,8-diazaspiro[4.5]decan-1-one수율 63.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 6344Dichloromethane용매

실험 절차

A suspension of rac-8-benzyl-4-phenyl-2,8-diaza-spiro[4.5]decan-1-one (28.8 g, 90 mmol) in MEOH:DCM (4:1, 500 mL) was hydrogenated in the presence of Pd (10% on C, 14 g, 132 mmol) at 2 bar for 48 h at room temperature. After filtration over celite, the reaction mixture was evaporated and the residue dissolved in NaOH (2 N, 200 mL). The product was extracted with DCM (3×150 mL) and the combined organic extracts dried over sodium sulfate. Filtration and evaporation afforded the title compound (13.1 g, 63%) as a white solid after trituration from diethylether. MS: m/e=231.4 (M+H).

후처리

  1. filtrationAfter filtration over celite
  2. customthe reaction mixture was evaporated
  3. dissolutionthe residue dissolved in NaOH (2 N, 200 mL)
  4. extractionThe product was extracted with DCM (3×150 mL)
  5. dry with materialthe combined organic extracts dried over sodium sulfate
  6. filtrationFiltration and evaporation

출처 및 근거

ORD 기록
ord-96bb75368eb4400f9f2bfc2348e5a09a
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07173133B2

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