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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661080Generated: October 26, 2026

Sodium Iodide → 1-(3-(5-Fluoro-2,3-dihydrospiro[indene-1,3'-pyrrolidine]-1'-yl)propyl)-5-(thiophen-2-yl)pyrimidine-2,4(1h,3h)-dione hydrochloride

https://huagongshe.com/reaction/1661080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3-chloropropyl)-5-(2-thienyl)-2,4(1H,3H)-pyrimidinedioneHCID 59337593—
Reactant5-Fluoro-2,3-dihydrospiro[indene-1,3'-pyrrolidine]hydrochloride saltHCID 67429481—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(3-(5-Fluoro-2,3-dihydrospiro[indene-1,3'-pyrrolidine]-1'-yl)propyl)-5-(thiophen-2-yl)pyrimidine-2,4(1h,3h)-dione hydrochlorideHCID 6742903572.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1-(3-chloropropyl)-5-(thiophen-2-yl)pyrimidine-2,4(1H,3H)-dione (Prep24, 50 mg, 0.18 mmol), 5-fluoro-2,3-dihydrospiro[indene-1,3′-pyrrolidine]hydrochloride salt (Prep14, 52 mg, 0.27 mmol), potassium carbonate (112 mg, 0.81 mmol), sodium iodide (112 mg, 0.75 mmol) and NMP (1 ml) was stirred at 70° C. overnight. The mixture was diluted with water and extracted with ethyl acetate. The EA phase was evaporated and the crude purified by preparative TLC to give the free base of the title compound (60 mg). the compound was purified by preparative HPLC and treated with a 1N solution of HCl-ether to give the title compound (6 mg, y=7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030322B2
Source datasetuspto-grants-2011_10
ORD IDord-20e867a4e05640f58e6078b6cc1166bb
Source noteuspto-grants-2011_10