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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434827Generated: October 31, 2026

Ammonia → 3-amino-N-(5-chloropyridin-2-yl)pyridine-2-carboxamide

https://huagongshe.com/reaction/1434827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantN-(5-chloropyridin-2-yl)-3-(trifluoroacetyl)amino-pyridine-2-carboxamideHCID 86619994—
SolventMethanolHCID 887—
Product3-amino-N-(5-chloropyridin-2-yl)pyridine-2-carboxamideHCID 11557851100%

Reaction Conditions

Temperature50 °C

Reaction Steps

To N-(5-chloropyridin-2-yl)-3-(trifluoroacetyl)amino-pyridine-2-carboxamide (1 g, 2.9 mmol) was added 5 mL of 2 M NH3 in MeOH. The reaction vessel was capped and heated to 50° C. for 12 h. The reaction mixture was cooled to 0° C. for 30 min and filtered to provide N-(5-chloropyridin-2-yl)-3-aminopyridine-2-carboxamide (0.72 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615568B2
Source datasetuspto-grants-2009_11
ORD IDord-71e8b26fada04d0f84a87b86a2d465d7
Source noteuspto-grants-2009_11