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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854264Generated: October 31, 2026

Water → (2-chloro-4-pyrimidinyl)(3-methyl-1,3-benzothiazol-2(3H)-ylidene)ethanenitrile

https://huagongshe.com/reaction/854264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 395229HCID 395229—
SolventDimethyl SulfoxideHCID 679—
Product(2-chloro-4-pyrimidinyl)(3-methyl-1,3-benzothiazol-2(3H)-ylidene)ethanenitrileHCID 728061985%

Reaction Steps

To a solution of 1 (0.1 g, 0.35 mmol) in dry DMSO was added dry K2CO3 then methyl iodide and the suspension was shaken at rt. for 2 days. The precipitate formed by addition of water was filtered off then washed with water until neutral pH. The crude residue, dried under vacuum at 40° C., was triturated in warm acetonitrile, filtered off then dried under vacuum at 40° C., affording 5.6 mg (5%) of the title compound as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259162B2
Source datasetuspto-grants-2007_08
ORD IDord-2c2c8c3e997646b4bb045e10cbeefc6e
Source noteuspto-grants-2007_08