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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661079Generated: October 27, 2026

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

https://huagongshe.com/reaction/1661079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-chlorobutyl)-5-(thiophen-2-yl)pyrimidine-2,4(1H,3H)-dioneHCID 59233926—
Reactant5-Chloro-2,3-dihydrospiro[indene-1,3'-pyrrolidine] hydrochlorideHCID 67427992—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(4-(5-Chloro-2,3-dihydrospiro[indene-1,3'-pyrrolidine]-1'-yl)butyl)-5-(thiophen-2-yl)pyrimidine-2,4(1h,3h)-dione hydrochlorideHCID 6742856781.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1-(4-chlorobutyl)-5-(thiophen-2-yl)pyrimidine-2,4(1H,3H)-dione (Prep23, 50 mg, 0.18 mmol), 5-chloro-2,3-dihydrospiro[indene-1,3′-pyrrolidine]hydrochloride (Prep10, 66 mg, 0.27 mmol), potassium carbonate (112 mg, 0.81 mmol), sodium iodide (108 mg, 0.72 mmol) and NMP (1 ml) was stirred at 70° C. overnight. Then it was cooled down to room temperature and diluted with water and extracted with ethyl acetate. The EA phase was evaporated and the crude purified by preparative TLC (TLC analysis performed by eluting with EA) to give the free base of the title compound (72 mg). The compound was purified by preparative HPLC and treated with a 1N solution of HCl-ether and freeze-dried give the title compound (51 mg, y=58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030322B2
Source datasetuspto-grants-2011_10
ORD IDord-e6696fba71d84ab3bbff136e7b725cff
Source noteuspto-grants-2011_10