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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848001Generated: November 3, 2026

Methyl iodide → 6-Ethynyl-2-(methylsulfanyl)-1,3-benzothiazole

https://huagongshe.com/reaction/1848001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Ethynylbenzo[d]thiazole-2-thiolHCID 178435587—
SolventDimethylformamideHCID 6228—
Product6-Ethynyl-2-(methylsulfanyl)-1,3-benzothiazoleHCID 86681026139.2%

Reaction Steps

To a stirred solution of 6-ethynylbenzo[d]thiazole-2-thiol (4.0 g, 21 mmol) from Step 2 of this Example in 20 mL of DMF at 0° C. were added K2CO3 (7.25 g, 5.25 mmol), and MeI (5 mL). The mixture was stirred at rt for 2 h before it was partitioned between EtOAc and water, the organic layer was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with 3:1 DCM/hexanes to afford 6-ethynyl-2-(methylthio)benzo[d]thiazole (1.5 g, 35%) as an off-white solid. LCMS (ESI) m/z 206 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952058B2
Source datasetuspto-grants-2015_02
ORD IDord-40a5b781406145f5815f9eec6948f17a
Source noteuspto-grants-2015_02