Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272191Generated: October 29, 2026

Tetrahydrofuran → HCID 58487036, compound

https://huagongshe.com/reaction/2272191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant2-Fluorobenzoyl chlorideHCID 9808—
Reactant3-Bromopyridine-2,6-diamineHCID 1415868—
SolventDichloromethaneHCID 6344—
ProductHCID 58487036HCID 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 numberUS09120751B2
Source datasetuspto-grants-2015_09
ORD IDord-fbb468b0f2cd4f9ab2a189a90ebb9587
Source noteuspto-grants-2015_09