Ammonia → 6-Chloro-5-(trifluoromethyl)pyridin-2-amine

Temperature

93 °C

2,6-Dichloro-3-(trifluoromethyl)pyridine (5.00 g, 23.2 mmol) and 28% aqueous ammonia (150 mL) were placed in a 250 mL autoclave. The mixture was heated at 93° C. for 21 h. The reaction was cooled to rt and extracted with EtOAc (100 mL×3). The combined organic extracts were dried over anhydrous Na2SO4 and evaporated under vacuum to give the crude product, which was purified by column chromatography on silica gel (2-20% EtOAc in petroleum ether as eluant) to give 6-chloro-5-(trifluoromethyl)pyridin-2-amine (2.1 g, 46% yield). 1H NMR (400 MHz, DMSO-d6) δ 7.69 (d, J=8.4 Hz, 1 H), 7.13 (br s, 2 H), 6.43 (d, J=8.4 Hz, 1 H). MS (ESI) m/z (M+H)+ 197.2

1. temperatureThe reaction was cooled to rt
2. extractionextracted with EtOAc (100 mL×3)
3. dry with materialThe combined organic extracts were dried over anhydrous Na2SO4
4. customevaporated under vacuum
5. customto give the crude product, which
6. customwas purified by column chromatography on silica gel (2-20% EtOAc in petroleum ether as eluant)

ORD record

ord-b8bc2728606a45369dfe4f85813aed38

Source dataset

uspto-grants-2015_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09216969B2