반응식
[CH3:1][N:2]1[C:6]([CH3:7])=[N:5][N:4]=[N:3]1.C([Li])CCC.[F:13][C:14]1[CH:27]=[CH:26][C:17]([C:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[O:19])=[CH:16][CH:15]=1>C1COCC1.CCCCCC>[F:13][C:14]1[CH:15]=[CH:16][C:17]([C:18]([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)([OH:19])[CH2:7][C:6]2[N:2]([CH3:1])[N:3]=[N:4][N:5]=2)=[CH:26][CH:27]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
A solution of 1,5-dimethyltetrazole (29.25 g; 0.298 mole) in dry THF (400 mL) was cooled to -78° C. and treated with n-butyllithium (133 mL of a 2.5M solution in hexane; 0.3325 mole) over 30 minutes. The mixture was stirred at -78° C. for 30 minutes and treated with 4-fluorobenzophenone (50 g, 0.25 mole. The mixture was stirred at -78° C. for 30 minutes and allowed to warm up to 23° C. over 2 hours. The reaction was quenched with 2N HCl (100 mL) and the organic solvent was removed by evaporation. The residue was extracted with CHCl3 (2×100 mL) and the combined organic layers were dried (Na2SO4) and evaporated to afford a brown oil. Purification by chromatography using 20% EtOAc-hexane as eluent afforded the title compound as a white solid (46.3 g; 62%). m.p.=113°-114° C. (crystallized from EtOAc-hexane). MS (CI): m/e=299 for (M+H)+ ;
후처리
- stirringThe mixture was stirred at -78° C. for 30 minutes
- temperatureto warm up to 23° C. over 2 hours
- customThe reaction was quenched with 2N HCl (100 mL)
- customthe organic solvent was removed by evaporation
- extractionThe residue was extracted with CHCl3 (2×100 mL)
- dry with materialthe combined organic layers were dried (Na2SO4)
- customevaporated
- customto afford a brown oil
- customPurification by chromatography
출처 및 근거
- ORD 기록
- ord-cc3cde0bbb62497c868a9e9b7f8d26aa
- 출처 데이터셋
- uspto-grants-1991_11
- 특허 번호
- US05068346
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