反应详情

Prepared from 5-(4-Methyl-5-trifluoromethyl-isoxazol-3-yl)-thiophene-2-carboxylic acid and 2-chloroaniline by the method described in Example 2 Method B. The reaction mixture was evaporated in vacuo, triturated and filtered with the aid of water, then washed with an aqueous 1 N hydrochloric acid solution followed by water. The crude solid was then chromatographed on silica gel with EtOAc/hexanes (10 then 15%) as eluant to afford product as a colorless solid (42 mg, 43%). 1H NMR (CDCl3) 2.39 (d, J=1.3, 3H), 7.10 (td, J=7.9, 1.3, 1H), 7.33 (td, J=7.9, 1.3, 1H), 7.42 (dd, J=8.3, 1.8, 1H), 7.56 (d, J=4.0, 1H), 7.69 (d, J=4.0, 1H), 8.34 (s, 1H), 8.46 (dd, J=1.3, 1H). 13C NMR 8.0, 114.8, 118.7 (q, J=271), 123.2, 125.4, 128.2, 129.0, 129.3, 134.0, 134.3, 141.7, 155.5 (q, J=40), 157.8, 159.0. 19F NMR −63.1. LC/MS 7.19 min, [M+1]+ 387.

1. customThe reaction mixture was evaporated in vacuo
2. customtriturated
3. filtrationfiltered with the aid of water
4. washwashed with an aqueous 1 N hydrochloric acid solution
5. customThe crude solid was then chromatographed on silica gel with EtOAc/hexanes (10