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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626415Generated: October 31, 2026

Oxalyl chloride → Ethyl 7-(4-(6-bromopyridin-2-ylcarbamoyl)phenoxy)-6-chlorochroman-4-carboxylate

https://huagongshe.com/reaction/1626415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-6-bromopyridineHCID 300809—
Reactant4-(6-Chloro-4-(ethoxycarbonyl)chroman-7-yloxy)benzoic acidHCID 58244395—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductEthyl 7-(4-(6-bromopyridin-2-ylcarbamoyl)phenoxy)-6-chlorochroman-4-carboxylateHCID 86664393—

Reaction Steps

4-(6-Chloro-4-(ethoxycarbonyl)chroman-7-yloxy)benzoic acid (1 g, 2.65 mmol) was diluted with DCM (10 mL) followed by the addition of oxalyl chloride in DCM (2M) (1.46 mL, 2.92 mmol) and DMF (1 drop). After stirring for 20 minutes, 6-bromopyridin-2-amine (0.505 g, 2.92 mmol) and DIEA (1.16 mL, 6.64 mmol) were added and the reaction was stirred overnight at ambient temperature. The reaction was loaded directly onto a biotage 40 cartridge and eluted with 5% ethyl acetate/hexanes to 70% ethyl acetate/hexanes to provide the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785445B2
Source datasetuspto-grants-2014_07
ORD IDord-f27019db60dc4b83813d1d1256e87504
Source noteuspto-grants-2014_07