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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396696Generated: November 3, 2026

Benzyl Bromide → HCID 66759164, compound

https://huagongshe.com/reaction/1396696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
ReactantHCID 178509029HCID 178509029—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 66759164HCID 6675916460.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5-amino-2-(4-fluorophenyl)thiazolo[5,4-d]pyrimidine-7-thiol (50 mg, 0.18 mmol) and triethylamine (63 μl, 0.45 mmol) in DMSO (1 ml) was added benzyl bromide (43 μl, 0.36 mmol). The reaction mixture was stirred under N2 at 25° C. for 3 hours. The mixture was poured onto water and extracted with EtOAc. The organic extracts were dried over Na2SO4 and the solvents were removed under reduced pressure. The residue was purified by flash chromatography on silica (CH2Cl2/MeOH 100:1) to yield the title compound as a light yellow solid (40 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901132B2
Source datasetuspto-grants-2014_12
ORD IDord-57257d07c48d4b898aa2fef1e45fa98b
Source noteuspto-grants-2014_12