Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591193Generated: November 4, 2026

6-Chloro-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione → HCID 19045431, compound

https://huagongshe.com/reaction/1591193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-1,3-dimethyl-2,4(1H,3H)-pyrimidinedioneHCID 81442—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloroethylamine hydrochlorideHCID 9793737—
ReactantHCID 16643157HCID 16643157—
SolventAcetonitrileHCID 6342—
ProductHCID 19045431HCID 1904543110.5%

Reaction Steps

A suspension of 3,4-dihydro-6-methoxyspiro[(2H)-1-benzopyran-2,4'-piperidin]-4-one (0.284 g, 1 mmol) and sodium bicarbonate (0.42 g, 5 mmol) in acetonitrile was heated at reflux for 1 hour, 2-chloro ethylamine hydrochloride (0.116 g, 1 mmol) was added the solution was heated at reflux for 17 hours, 6-chloro-1,3-dimethyluracil (0.175 g, 1 mmol) and sodium bicarbonate (0.16 g, 2 mmol) were added. Refluxing was continued for 28 hours. After cooling, the reaction mixture was concentrated in vacuo to dryness. The residue was partitioned between chloroform and water. The chloroform solution was washed with water and dried over sodium sulfate. The resulting residue was chromatographed through a pressure column (silica gel) eluting with 5% methanol/chloroform to give the title compound (45 mg, 10.5% yield), mp 235°-238° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206240
Source datasetuspto-grants-1993_04
ORD IDord-13364849411040d1a91bbd1e10451169
Source noteuspto-grants-1993_04