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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73797Generated: October 29, 2026

Dimethylformamide → 5-bromo-6-chloro-N-(4-(1,1-difluoroethoxy)phenyl)nicotinamide

https://huagongshe.com/reaction/73797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromo-6-chloropyridine-3-carboxylic acidHCID 285433—
ReactantBenzenamine, 4-(1,1-difluoroethoxy)-HCID 68195912—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-bromo-6-chloro-N-(4-(1,1-difluoroethoxy)phenyl)nicotinamideHCID 86702629—

Reaction Steps

Oxalyl chloride (653 μL, 7.46 mmol) was added to a mixture of 5-bromo-6-chloronicotinic acid (1.2 g, 4.97 mmol) and DMF (20 μL, 0.258 mmol) in DCM (40 mL) under nitrogen atmosphere and the RM was stirred for 2 h at RT. The solvent was evaporated, the residue was dissolved in DCM (10 mL) and evaporated again to dryness. The residue was dissolved in THF (30 mL), DIPEA (1.737 mL, 9.95 mmol) was added and the RM was cooled down to −15° C. 4-(1,1-difluoroethoxy)aniline (Stage 30.3, 0.932 g, 5.22 mmol) in THF (10 mL) was added dropwise in 15 min. period and the RM was stirred for 1 h at RT. The solvent was evaporated off under reduced pressure and the residue was diluted with EtOAc (100 mL), treated with citric acid 10% (60 mL) and extracted with EtOAc. The combined extracts were washed with sat. aq. Na2CO3 (50 mL) and brine (2×50 mL), dried over Na2SO4 and the solvent was evaporated off under reduced pressure to give the crude product which was suspended in n-hexane, filtered and dried to give the title product as a beige solid. HPLC (Condition 5) tR=7.3 min, UPLC-MS (Condition 3) tR=1.16 min, m/z=391/393 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829195B2
Source datasetuspto-grants-2014_09
ORD IDord-4d7b8e4564de4fda824523e6578c81bc
Source noteuspto-grants-2014_09