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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828728Generated: November 1, 2026

Triethylamine → 2-chloro-N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-4-carboxamide

https://huagongshe.com/reaction/1828728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloropyridine-4-carbonyl chlorideHCID 2800003—
ReactantN-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamideHCID 17904941—
SolventDichloromethaneHCID 6344—
Product2-chloro-N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-4-carboxamideHCID 2205795090.4%

Reaction Steps

2-Chloropyridine-4-carbonyl chloride (0.143 g) was added to a stirred mixture of N-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamide (0.211 g), triethylamine (0.164 g) and methylene chloride (10 ml) and the mixture was stirred at ambient temperature for 16 hours. The precipitate was isolated, washed with a saturated aqueous sodium bicarbonate solution and with methylene chloride and dried under vacuum at 40° C. There was thus obtained the title compound (0.276 g); NMR Spectrum: (DMSOd6) 2.2 (s, 3H), 3.50-3.53 (m, 4H), 3.69-3.73 (m, 4H), 7.08 (d, 1H), 7.24 (d, 2H), 7.34 (d, 1H) 7.81 (s, 1H), 7.88 (d, 1H), 7.98 (s, 1H), 8.26 (d, 1H), 8.6 (d, 1H); Mass Spectrum M+H+ 452 and 454.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060700B2
Source datasetuspto-grants-2006_06
ORD IDord-aa078c60129d4a6189e0f422724a6735
Source noteuspto-grants-2006_06