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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036093Generated: October 31, 2026

Tetrahydrofuran → N-(6-amino-5-bromo(2-pyridyl))(2-fluorophenyl)carboxamide

https://huagongshe.com/reaction/1036093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant2-Fluorobenzoyl chlorideHCID 9808—
Reactant3-Bromopyridine-2,6-diamineHCID 1415868—
SolventDichloromethaneHCID 6344—
ProductN-(6-amino-5-bromo(2-pyridyl))(2-fluorophenyl)carboxamideHCID 5848703657%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3-bromo-2,6-diaminopyridine (60) (564 mg, 3 mmol), triethyl amine (0.54 ml) in DCM (6 ml)/THF (4 ml) was cooled down to −78° C. A solution of 2-fluorobenzoyl chloride (362 μl, 3.03 mmol) in 2 ml DCM was added dropwise within 10 min. The resulting reaction mixture was stirred at −78° C. for 1 h before slowly warm up to r.t. After stirred at r.t. for 3 h, the reaction quenched with aq NaHCO3 solution. 200 ml EA were added. Org. phase was washed with brine, dried over sodium sulfate, concentrated. The light yellow solid residue was triturated with DCM (ca. 15 ml), filtered and dried to give 530 mg N-(6-amino-5-bromo(2-pyridyl))(2-fluorophenyl)carboxamide (61) as white solid. (purity>95%, yield: 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546403B2
Source datasetuspto-grants-2013_10
ORD IDord-cbff9cb88fc74f5c855f30c367f1ead2
Source noteuspto-grants-2013_10