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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048057Generated: October 26, 2026

Tranylcypromine → methyl 7-(4-((2-phenylcyclopropyl)carbamoyl)phenoxy)-6-cyano-3,4-dihydro-2H-chromene-4-carboxylate

https://huagongshe.com/reaction/1048057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTranylcypromineHCID 5530—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(6-Cyano-4-(methoxycarbonyl)-chroman-7-yloxy)benzoic acidHCID 46221108—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Productmethyl 7-(4-((2-phenylcyclopropyl)carbamoyl)phenoxy)-6-cyano-3,4-dihydro-2H-chromene-4-carboxylateHCID 67080429—

Reaction Steps

To a solution of 4-(6-cyano-4-(methoxycarbonyl)chroman-7-yloxy)benzoic acid (Preparation 2) (21.8 mg, 0.0617 mmol) in dichloromethane (1 ml) with a drop of DMF was added oxalyl chloride (2M in dichloromethane) (0.0370 ml, 0.0740 mmol). Gas evolution was observed. The mixture was stirred for 0.5 hours at ambient temperature. Triethylamine (0.0430 ml, 0.3085 mmol) and 2-phenylcyclopropanamine, hemisulfate (28.11 mg, 0.1542 mmol) were added sequentially to the mixture. The mixture was stirred for 17 hours at ambient temperature. The crude mixture was purified on silica gel (MeOH in dichloromethane gradient) to provide 25.9 mg of the title compound as a thin film (90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569522B2
Source datasetuspto-grants-2013_10
ORD IDord-04aa2cc99ad04aadb7ddcce1f3ec04c7
Source noteuspto-grants-2013_10