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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848002Generated: October 30, 2026

Formaldehyde → 6-(Imidazo[1,2-a]pyridin-3-ylmethyl)-2-(methylthio)benzo[d]thiazole

https://huagongshe.com/reaction/1848002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-AminopyridineHCID 10439—
Reactant6-Ethynyl-2-(methylsulfanyl)-1,3-benzothiazoleHCID 86681026—
CatalystCuprous chlorideHCID 62652—
Catalystcopper(II) trifluoromethanesulfonateHCID 2734996—
SolventTolueneHCID 1140—
Product6-(Imidazo[1,2-a]pyridin-3-ylmethyl)-2-(methylthio)benzo[d]thiazoleHCID 8668102738%

Reaction Conditions

Temperature120 °C

Reaction Steps

A stirred mixture of 2-aminopyridine (100 mg, 1.1 mmol), paraformaldehyde (34 mg, 1.1 mmol), CuCl (5 mg, 0.06 mmol), and Cu(OTf)2 (19 mg, 0.06 mmol) in 3 mL of toluene in a pressure tube was flushed with argon. 6-Ethynyl-2-(methylthio)benzo[d]thiazole (327 mg, 1.6 mmol) from Step 3 of this Example was added. The reaction vessel was sealed and the mixture was heated in an oil bath at 120° C. for 6 h. LCMS analysis showed that the reaction was mostly complete. The reaction mixture was partitioned between EtOAc and saturated aq NaHCO3. 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 0-100% EtOAc in hexanes to afford 6-(imidazo[1,2-a]pyridin-3-ylmethyl)-2-(methylthio)benzo[d]thiazole (127 mg, 38%) as a brown oil. LCMS (ESI) m/z 312 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952058B2
Source datasetuspto-grants-2015_02
ORD IDord-36ffaa4090384c57935bbcd0a0b18781
Source noteuspto-grants-2015_02