반응 #595315
ord-f6f4f8c6e8ed439db03eb2259eb8c561
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반응물
시약
반응 조건
후처리
- 1온도to warm to −20° C. over 1 h
- 2기타quenched with water
- 3추출extracted with dichloromethane
- 4추출The combined organic extract
- 5세척was washed with aqueous 1.0 N of NaOH and brine
- 6건조dried with anhydrous sodium sulfate
- 7농축concentrated
- 8기타The residue was purified by column chromatography on silica gel
실험 절차
To a stirred solution of dimethylsulfoxide (38 mg) in dichloromethane (1 mL) at −60° C. was added trifluoroacetic anhydride (105 mg). After the reaction mixture was stirred for 10 minutes at −60° C., a solution of 4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-1-naphthalenecarboxamide (75 mg, in 1.5 mL of dichloromethane and 0.4 mL of dimethylsulfoxide) was added. The reaction mixture was allowed to warm to −20° C. over 1 h, then quenched with water and extracted with dichloromethane. The combined organic extract was washed with aqueous 1.0 N of NaOH and brine, dried with anhydrous sodium sulfate and concentrated. The residue was purified by column chromatography on silica gel using dichloromethane/methanol (98:2 to 95:5) as eluent to afford the title product, a compound of the present invention, as semi-solid (70 mg, 82% yield).