Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626533Generated: October 31, 2026

Oxalyl chloride → HCID 67287554, compound

https://huagongshe.com/reaction/1626533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(6-Chloro-4-(ethoxycarbonyl)chroman-7-yloxy)benzoic acidHCID 58244395—
ReactantHCID 67288108HCID 67288108—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 67287554HCID 6728755425.8%

Reaction Steps

4-(6-Chloro-4-(ethoxycarbonyl)chroman-7-yloxy)benzoic acid (Preparation B; 200 mg, 0.531 mmol) was diluted with dichloromethane (2 mL) followed by the addition of oxalyl chloride in dichloromethane (2M) (292 μL, 0.584 mmol) and dimethylformamide (1 drop). After stirring for 15 minutes, 3-(2-aminoethyl)-6-cyclopropyl-N,N-dimethylpyridin-2-amine (109 mg, 0.531 mmol) and diisopropyl ethylamine (277 μL, 1.59 mmol) were added. After stirring for 2 hours, the reaction was loaded onto silica gel and eluted with 5% ethyl acetate/hexanes to 100% ethyl acetate to yield ethyl 6-chloro-7-(4-(2-(6-cyclopropyl-2-(dimethylamino)pyridin-3-yl)ethylcarbamoyl)phenoxy)chroman-4-carboxylate (77 mg, 0.137 mmol, 25.7% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785445B2
Source datasetuspto-grants-2014_07
ORD IDord-f3a9553209504fb1bb2f0c4e88f08c95
Source noteuspto-grants-2014_07