Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → (1R*,2R*,5S*,6R*)-8-Benzyl-2-[3,5-bis(trifluoromethyl)benzoyloxy]-1-phenyl-6-phenylsulphonyl-8-azabicyclo[3.2.1]octane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3,5-Bis(trifluoromethyl)benzoyl chloride | HCID 101856 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (1R*,2R*,5S*,6R*)-8-Benzyl-1-phenyl-6-phenylsulphonyl-8-azabicyclo[3.2.1]octan-2-ol | HCID 69890353 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (1R*,2R*,5S*,6R*)-8-Benzyl-2-[3,5-bis(trifluoromethyl)benzoyloxy]-1-phenyl-6-phenylsulphonyl-8-azabicyclo[3.2.1]octane | HCID 86586643 | 69.3% |
반응 단계
A solution of (1R*,2R*,5S*,6R*)-8-benzyl-1-phenyl-6-phenylsulphonyl-8-azabicyclo[3.2.1]octan-2-ol (Description 4; 0.98 g, 2.25 mmol), triethylamine (0.6 ml), N,N-dimethylaminopyridine (100 mg) and 3,5-bis(trifluoromethyl)benzoyl chloride (0.6 ml, 3.33 mmol) in dry dichloromethane (10 ml) was stirred at room temperature for 6 days. The reaction mixture treated with saturated aqueous NaHCO3 and extracted with dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified by chromatography on silica gel (iso-hexane:ethyl acetate 5-30%) to give the title compound (1.05 g, 69%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06727249B2 |
| 출처 데이터셋 | uspto-grants-2004_04 |
| ORD ID | ord-5fd95c5c464b49d0a243b45da076a18a |
| 출처 메모 | uspto-grants-2004_04 |