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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510815Generated: October 26, 2026

Trisodium phosphate dodecahydrate → N-(2-Chloro-4-methylpyridin-3-yl)-2-(cyclopropylamino)nicotinamide

https://huagongshe.com/reaction/1510815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrisodium phosphate dodecahydrateHCID 61473—
ReactantCyclopropylamineHCID 69828—
Reactant2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridinecarboxamideHCID 10423868—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
ProductN-(2-Chloro-4-methylpyridin-3-yl)-2-(cyclopropylamino)nicotinamideHCID 9972204—

Reaction Conditions

Temperature135 °C

Reaction Steps

2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridine carboxamide (50 g), trisodium phosphate dodecahydrate (67.37 g), cyclopropylamine (40.43 g) were suspended in o-xylene (150 ml) and heated to 130-140° C. for 6-8 h in autoclave. Then the reaction mass was cooled to 70-75° C., diluted with o-xylene (250 ml) and DM water (150 ml) and stirred for 10 min at 70-80° C. The aqueous layer was separated and washed the organic layer with DM water (150 ml) at 70-80° C. The organic layer was concentrated at 60-65° C. under reduced pressure up to residual weight attained is approximately 200 g. The concentrated mass was cooled to 5-10° C. and stirred for 30 min. Filtered the solid obtained and washed with chilled o-xylene (50 ml, 5-10° C.). Dried the obtained solid at 55-60° C. under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212025B2
Source datasetuspto-grants-2012_07
ORD IDord-b09d27de43274c5cb66395f3b37008e6
Source noteuspto-grants-2012_07