반응 #45618

반응 방정식

ethyl acetate

triethylamine

(3S)-3-methylaminopyrrolidine

2-Cyclopropyl-7-fluoro-5-methyl-6-(2-methyl-1,3-thiazol-4-yl)-1,3-benzoxazole-4-carbonitrile

→

compound

수율 17.5%

2-Cyclopropyl-7-[(3S)-3-(methylamino)pyrrolidin-1-yl]-5-methyl-6-(2-methyl-1,3-thiazol-4-yl)-1,3-benzoxazole-4-carbonitrile

수율 17.5%

용매

water

dimethyl sulfoxide

반응 조건

후처리

1. 1
   온도After cooling to room temperature
2. 2
   세척The organic layer was washed with saturated brine
3. 3
   건조dried over anhydrous sodium sulfate
4. 4
   기타The solvent was evaporated away
5. 5
   세척eluted with a mixed solvent of chloroform/methanol (10:1
6. 6
   기타v/v) followed by recrystallization and purification with a mixed solvent of diethyl ether/ethyl acetate/n-hexane

실험 절차

2-Cyclopropyl-7-fluoro-5-methyl-6-(2-methyl-1,3-thiazol-4-yl)-1,3-benzoxazole-4-carbonitrile (I-80) (100 mg, 0.32 mmol) was dissolved in dimethyl sulfoxide (2 ml), triethylamine (112 μl, 0.80 mmol) and (3S)-3-methylaminopyrrolidine (44 μl, 0.42 mmol) were added, followed by stirring at 90° C. for 6 hours under nitrogen atmosphere. After cooling to room temperature, ethyl acetate was added, followed by fractionation with water. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate. The solvent was evaporated away and the resulting residue was subjected to preparative thin-layer silica gel column chromatography, eluted with a mixed solvent of chloroform/methanol (10:1, v/v) followed by recrystallization and purification with a mixed solvent of diethyl ether/ethyl acetate/n-hexane to obtain the entitled compound (22 mg, 17%) as a white solid.

출처