참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenyl isocyanate | HCID 7672 | — |
| 반응물 | 1-Nitrobutane | HCID 12302 | — |
| 반응물 | 7a-ethynylhexahydro-1H-pyrrolizine | HCID 19597695 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 7a-(3-propyl-5-isoxazolyl)-hexahydro-1H-pyrrolizine | HCID 18934724 | 53.4% |
반응 단계
Nitrobutane (0.705 mL, 6.66 mmol) and phenylisocyanate (1.50 mL, 13.3 mmol) were dissolved in benzene (13.5 mL) and added to a flask containing 7a-ethynyl-hexahydro-1H-pyrrolizine (450 mg, 3.33 mmol, from step 13a). The solution was stirred at ambient temperature for 1 hour and at reflux for 5 hours. The mixture was cooled, filtered, concentrated and diluted with EtOAc. The solution was extracted with 6N HCl. The aqueous phase was made basic with 15% NaOH and extracted with methylene chloride. The organic extracts were combined, dried (MgSO4) and concentrated. The residue was residue was chromatographed (silica gel; CHCl3 /MeOH, 98:2) to afford an amber oil (392 mg, 53%). 1H NMR (CDCl3, 300 MHz) δ0.97 (t, J=7.5 Hz, 3H), 1.61-1.92 (m, 8H), 2.15-2.26 (m, 2H), 2.55-2.69 (m, 4H), 3.13-3.20 (m, 2H), 5.96 (s, 1H); MS (CI/NH3) m/z: 221 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05733912 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-bbc0aabc6c144848bb5aa35cb5124c07 |
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| 출처 메모 | uspto-grants-1998_03 |
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