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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507795Generated: October 30, 2026

Methyl iodide → HCID 46916710, compound

https://huagongshe.com/reaction/1507795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 46916666HCID 46916666—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 46916710HCID 4691671074%

Reaction Steps

To a suspension of 5-amino-7-[4-(4-chlorophenoxyacetyl)piperazin-1-yl]-2-(4-chlorophenylmethyl)thiazolo[5,4-d]pyrimidine (53 mg, 0.1 mmol) in DMF (2 ml) was added 1N NaOH (150 μl, 0.15 mmol) and MeI (7 μl, 0.11 mmol). The resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with dichloromethane and washed with water and brine. The organic layer was evaporated in vacuo and purified by flash chromatography on silica, the mobile phase being a mixture of methanol and dichloromethane (in a ratio of 1/80), yielding the pure title compound (40 mg, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221822B2
Source datasetuspto-grants-2015_12
ORD IDord-cba57788b9a54211b9b366c2d6cf9d0b
Source noteuspto-grants-2015_12