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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889328Generated: October 31, 2026

Phenethylamine → 6-cyclopropyl-3-(2-phenylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1889328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamineHCID 1001—
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
ReactantMethyl 2-amino-5-cyclopropylthiophene-3-carboxylateHCID 45089420—
SolventDichloromethaneHCID 6344—
Product6-cyclopropyl-3-(2-phenylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 59351729108.6%

Reaction Steps

To a solution (15 mL) of methyl 2-amino-5-cyclopropylthiophene-3-carboxylate (0.5 g) in methylene chloride were added triphosgene (0.9 g) and triethylamine (1.5 mL), and the mixture was stirred at room temperature for 2 hr. To the reaction mixture was added 2-phenylethanamine (0.92 g), and the mixture was further stirred at room temperature for 1 hr. The reaction mixture was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in methanol (10 mL), sodium methoxide (0.5 g) was added, and the mixture was stirred at 60° C. for 2 hr. The reaction mixture was neutralized with hydrochloric acid (10% methanol solution), insoluble material was filtered off, and the solvent was evaporated under reduced pressure. The precipitated solid was collected by filtration to give the title compound as a colorless solid (0.86 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501750B2
Source datasetuspto-grants-2013_08
ORD IDord-8641f3aee54b43ef8929fbe1953a1d48
Source noteuspto-grants-2013_08