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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623771Generated: November 1, 2026

Triethylamine → 5-hydroxy-2-[(phenylmethyl)oxy]-N-3-pyridinylbenzamide

https://huagongshe.com/reaction/1623771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-AminopyridineHCID 10009—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(Benzyloxy)-5-hydroxybenzoic acidHCID 24771944—
SolventDichloromethaneHCID 6344—
Product5-hydroxy-2-[(phenylmethyl)oxy]-N-3-pyridinylbenzamideHCID 51357514—

Reaction Steps

Oxalyl chloride (1.08 ml, 12.28 mmol) was added to a mixture of 5-hydroxy-2-[(phenylmethyl)oxy]benzoic acid (1 g, 4.09 mmol) dissolved in dichloromethane. The mixture was stirred for 2 h, and then concentrated. The residue was dissolved in dichloromethane, and then added to a mixture of pyridin-3-amine (0.39 g, 4.09 mmol) and triethylamine (1.14 ml, 8.19 mmol) in dichloromethane. The mixture was stirred at 40° C. for 3 h. The mixture was filtered, and the filtrate was added to water (10 ml) and extracted with ethyl acetate (30 ml). The organic phase was concentrated to yield the title compound as a crude solid product. 0.72 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-a8fc597cb15046aeb2447e30592cd120
Source noteuspto-grants-2014_07