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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379577Generated: October 30, 2026

Water → 6-[(1H-Benzimidazol-1-yl)methyl]-3-methyl-1-(1-methylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/379577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzimidazoleHCID 5798—
ReactantPotassium CarbonateHCID 11430—
Reactant6-(chloromethyl)-3-methyl-1-(1-methylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 18366626—
SolventDimethylformamideHCID 6228—
Product6-[(1H-Benzimidazol-1-yl)methyl]-3-methyl-1-(1-methylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 1836661955.1%

Reaction Steps

Benzimidazole (0.395 g) and potassium carbonate (1 g) were added to a stirred solution of 6-(chloromethyl)-3-methyl-1-(1-methylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (0.55 g) in anhydrous dimethylformamide (5 ml) at room temperature. After 2 days, water (50 ml) was added and the mixture was extracted with ethyl acetate (2×50 ml). The organic extracts were dried over anhydrous magnesium sulfate and filtered through a silica pad which was washed with ethyl acetate. The filtrate was evaporated and the residue was purified twice by normal-phase preparative HPLC with gradient dichloromethane/ethanol elution to give the title compound (0.394 g) as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300334B1
Source datasetuspto-grants-2001_10
ORD IDord-860c5f7c6b3143889ba5de956e569417
Source noteuspto-grants-2001_10