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Pyridine → (S)-alpha-Methyl-N-(4-oxo-1-phenylcyclohexyl)-3,5-bis(trifluoromethyl)benzeneacetamide

HRID 2213056
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HRID 2213056 반응식
O=C1N(P(Cl)(N2CCOC2=O)=O)CCO1.[CH3:16][C@@H:17]([C:21]1[CH:26]=[C:25]([C:27]([F:30])([F:29])[F:28])[CH:24]=[C:23]([C:31]([F:34])([F:33])[F:32])[CH:22]=1)[C:18](O)=[O:19].N1C=CC=CC=1.Cl.[O:42]=[C:43]1[CH2:48][CH2:47][C:46]([NH2:55])([C:49]2[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=2)[CH2:45][CH2:44]1>ClCCl>[CH3:16][C@@H:17]([C:21]1[CH:22]=[C:23]([C:31]([F:32])([F:34])[F:33])[CH:24]=[C:25]([C:27]([F:29])([F:30])[F:28])[CH:26]=1)[C:18]([NH:55][C:46]1([C:49]2[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=2)[CH2:45][CH2:44][C:43](=[O:42])[CH2:48][CH2:47]1)=[O:19]
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참가 물질

6

반응물 4

HCID 1049PyridineHCID 152842Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 219552264-Oxo-1-phenylcyclohexylamine hydrochlorideHCID 86590573(S)-alpha-Methyl-3,5-bis(trifluoromethyl)benzeneacetic Acid

생성물 1

HCID 86590577(S)-alpha-Methyl-N-(4-oxo-1-phenylcyclohexyl)-3,5-bis(trifluoromethyl)benzeneacetamide수율 37%

시약·촉매·용매

1
HCID 6344Dichloromethane용매2회

실험 절차

Bis(2-oxo-3-oxazolidinyl)phosphinic chloride (672 mg, 2.64 mmol) was added to a solution of (S)-α-methyl-3,5-bis(trifluoromethyl)benzeneacetic acid (Description 40, 500 mg, 1.76 mmol) and pyridine (284 μL, 3.52 mmol) in dichloromethane (15 mL) and the mixture was stirred at room temperature for 5 minutes. 4-Oxo-1-phenylcyclohexylamine hydrochloride (Description 18, 500 mg, 2.64 mmol) was added and the mixture was stirred at room temperature for 48 hours. The mixture was diluted with dichloromethane and washed with saturated aqueous sodium carbonate. The organic layer was dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with isohexane:EtOAc (65:35). The residue was crystallised twice from propan-2-ol/water (50:50, 20 mL) and the solid was collected and dried in vacuo to give the title compound as a colorless solid (200 mg, 37%). 1H NMR (400 MHz, CDCl3) δ 7.80 (1H, s), 7.72 (2H, s), 7.29 (5H m), 5.71 (1H, s), 3.70 (1H, q, J 7.0 Hz), 2.81 (1H, m), 2.64 (1H, m), 2.47–2.04 (5H, m), 1.60 (1H, m), and 1.52 (3H, d, J 7.0 Hz). e.e. [Determined by chiral HPLC (Chiralcel OD-H 250×4.6 mm i.d.; isohexane/EtOH (96:4); 1 mL/min; 210 nm]>99%.

후처리

  1. stirringthe mixture was stirred at room temperature for 48 hours
  2. washwashed with saturated aqueous sodium carbonate
  3. dry with materialThe organic layer was dried (MgSO4)
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by flash column chromatography on silica gel
  6. washeluting with isohexane:EtOAc (65:35)
  7. customThe residue was crystallised twice from propan-2-ol/water (50:50, 20 mL)
  8. customthe solid was collected
  9. customdried in vacuo

출처 및 근거

ORD 기록
ord-beea6d8fa08e465fb697ce07e82c6013
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07105507B2

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