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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58296Generated: October 25, 2026

Water → 7-(1-azidoethyl)-6-(2-chlorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/58296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chlorophenylboronic acidHCID 2734322—
Reactant7-(1-azidoethyl)-6-bromo-3-methyl-5H-thiazolo[3,2-a]pyrimidin-5-oneHCID 58111438—
CatalystHCID 178482906HCID 178482906—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product7-(1-azidoethyl)-6-(2-chlorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-oneHCID 8665008247.2%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a mixture of 7-(1-azidoethyl)-6-bromo-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one (0.12 g, 0.38 mmol) and (2-chlorophenyl)boronic acid (0.072 g, 0.46 mmol) in 1,4-dioxane (3 mL) was added a 1 N solution of sodium carbonate in water (0.57 mL, 0.57 mmol) and dichloro(bis{di-tert-butyl[4-(dimethylamino)phenyl]phosphoranyl})palladium (0.014 g, 0.019 mmol). The mixture was stirred at 105° C. overnight. After cooling, the mixture was diluted with ethyl acetate, washed with water, dried over Na2SO4, concentrated, and purified on silica gel (0-30% ethyl acetate/hexanes) to give the desired product (0.062 g). LCMS calculated for C15H13ClN5OS (M+H)+: m/z=346.1. Found: 346.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434746B2
Source datasetuspto-grants-2016_09
ORD IDord-ac5d43e5eb7a4fe0a47f0e67039d3947
Source noteuspto-grants-2016_09