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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170413Generated: October 29, 2026

Triethylamine → 5-chloro-2-fluoro-N-(2-methoxy-4-pyridyl)benzamide

https://huagongshe.com/reaction/2170413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methoxypyridin-4-amineHCID 280891—
Reactant5-Chloro-2-fluorobenzoic acidHCID 2736537—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDichloromethaneHCID 6344—
Product5-chloro-2-fluoro-N-(2-methoxy-4-pyridyl)benzamideHCID 8672846847.3%

Reaction Steps

A solution of 5-chloro-2-fluoro-benzoic acid (5.0 g, 28.64 mmol), HATU (10.89 g, 28.64 mmol), 2-methoxypyridin-4-amine (3.6 g, 28.64 mmol) and Et3N (15.98 mL, 114.60 mmol) in dichloromethane (45.0 mL) was stirred at room temperature overnight. The crude mixture was purified by column chromatography eluting with a gradient of ethyl acetate in hexanes (0-50%) to yield 5-chloro-2-fluoro-N-(2-methoxy-4-pyridyl)benzamide (3.8 g, 47%) as a white solid. ESI-MS m/z calc. 280.04. found 281.3 (M+1)+; Retention time: 1.31 minutes (3 minutes run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051270B2
Source datasetuspto-grants-2015_06
ORD IDord-dc2dac72505b41d18c3a24cf0798d3b7
Source noteuspto-grants-2015_06