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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773324Generated: November 3, 2026

Water → 1-[(1,3-Benzothiazol-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-bromo-xanthine

https://huagongshe.com/reaction/1773324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Bromomethyl)-1,3-benzothiazoleHCID 2776258—
Reactant8-Bromo-7-(2-butyn-1-yl)-3,7-dihydro-3-methyl-1H-purine-2,6-dioneHCID 21088927—
SolventDimethylformamideHCID 6228—
Product1-[(1,3-Benzothiazol-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-bromo-xanthineHCID 11803499990%

Reaction Steps

By utilizing the well known method, 3-methyl-7-(2-butyn-1-yl)-8-bromo-xanthine 1a (327 mg, 1 mmol) was dissolved in N,N-dimethylformamide (5 ml). Potassium carbonate (221 mg, 1.6 mmol) and 2-bromomethyl-1,3-benzothiazole (228 mg, 1 mmol) were added to give a reaction mixture. The reaction mixture was reacted overnight at room temperature and TLC was used to monitor the reaction progress. After the reaction was completed, the obtained reaction mixture was poured into water, suction filtered, and the obtained solid was washed with water, dried to give 1-[(1,3-benzothiazol-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-bromo-xanthine 2b (400 mg, yellow solid), yield: 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255098B2
Source datasetuspto-grants-2016_02
ORD IDord-a344a0b6e1254354a8c6aa1abc01f6b4
Source noteuspto-grants-2016_02