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Sodium hydride → Benzyl [(9S)-11-oxo-9-phenyl-6,10-diazaspiro[4.6]undec-10-yl]acetate

HRID 1864936
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HRID 1864936 반응식
[H-].[Na+].[C:3]1([C@H:9]2[NH:19][C:18](=[O:20])[C:13]3([CH2:17][CH2:16][CH2:15][CH2:14]3)[NH:12][CH2:11][CH2:10]2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Br[CH2:22][C:23]([O:25][CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)=[O:24]>C1COCC1>[O:20]=[C:18]1[C:13]2([CH2:17][CH2:16][CH2:15][CH2:14]2)[NH:12][CH2:11][CH2:10][C@@H:9]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:19]1[CH2:22][C:23]([O:25][CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)=[O:24]
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참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 62576Benzyl bromoacetateHCID 66973323(9S)-9-phenyl-6,10-diazaspiro[4.6]undecan-11-one

생성물 1

HCID 86616407Benzyl [(9S)-11-oxo-9-phenyl-6,10-diazaspiro[4.6]undec-10-yl]acetate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
60 °C

실험 절차

To a suspension of sodium hydride (0.147 g, 6.14 mmol) in THF (10 mL) was added (9S)-9-phenyl-6,10-diazaspiro[4.6]undecan-11-one (0.300 g, 1.23 mmol) at ambient temperature. The reaction was warmed to 60° C. for 2 h, then cooled to ambient temperature. Benzyl bromoacetate (0.309 g, 1.35 mmol) was added dropwise to the reaction. After 1 h, the mixture was quenched with a saturated aqueous ammonium chloride solution. The mixture was concentrated in vacuo then partitioned between H2O and CH2Cl2. The aqueous phase was then extracted several times with CH2Cl2. The combined organic extracts were washed with saturated brine, then dried over MgSO4, filtered and concentrated in vacuo The residue was purified by silica gel chromatography, eluting with a gradient of EtOAc:hexane-0:100 to 100:0, to yield the title compound. MS: m/z=393 (M+1).

후처리

  1. temperaturecooled to ambient temperature
  2. customthe mixture was quenched with a saturated aqueous ammonium chloride solution
  3. concentrationThe mixture was concentrated in vacuo
  4. customthen partitioned between H2O and CH2Cl2
  5. extractionThe aqueous phase was then extracted several times with CH2Cl2
  6. washThe combined organic extracts were washed with saturated brine
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo The residue
  10. customwas purified by silica gel chromatography
  11. washeluting with a gradient of EtOAc

출처 및 근거

ORD 기록
ord-33e166f6158a4efd93be5e402930f1b5
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07625901B2

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