Ammonia → 3-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)propanimidamide

To a solution of 3-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenyl)propanenitrile (1 g, 3.07 mmol) in toluene (4 mL) and methanol (1 mL) was added dropwise AcCl (1.091 mL, 15.35 mmol) at 0° C. in 5 min. The mixture was stirred at room temperature for 2 h. The mixture was cooled to 0° C. in an ice bath, and ammonia (4.39 mL, 30.7 mmol) in methanol was added dropwise in 5 min. The mixture was stirred at room temperature overnight. The mixture was filtered to remove the solid, and the solid was washed with toluene (20 mL) and methanol (20 mL). The combined filtrate was concentrated in vacuo, the residue was triturated with diethyl ether, the resulting white solid was collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound (0.85 g, 2.242 mmol, 73.0% yield) as white solid. LCMS: rt=1.17 min, [M+H+]=343

1. temperatureThe mixture was cooled to 0° C. in an ice bath
2. stirringThe mixture was stirred at room temperature overnight
3. filtrationThe mixture was filtered
4. customto remove the solid
5. washthe solid was washed with toluene (20 mL) and methanol (20 mL)
6. concentrationThe combined filtrate was concentrated in vacuo
7. customthe residue was triturated with diethyl ether
8. filtrationthe resulting white solid was collected by filtration
9. washwashed with diethyl ether
10. customdried in vacuo

ORDレコード

ord-ea327b3cb552464da8df5251d7e4522b

出典データセット

uspto-grants-2015_11

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09174968B2