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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768371Generated: October 26, 2026

2-Chloro-1,1,1-triethoxyethane → 2-(Chloromethyl)-5-methoxy[1,3]thiazolo[5,4-b]pyridine

https://huagongshe.com/reaction/1768371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,1,1-triethoxyethaneHCID 305922—
Reactant3-Amino-6-methoxypyridine-2(1H)-thioneHCID 178492403—
SolventEthanolHCID 702—
Product2-(Chloromethyl)-5-methoxy[1,3]thiazolo[5,4-b]pyridineHCID 22065968—

Reaction Conditions

Temperature90 °C

Reaction Steps

3-Amino-6-methoxy-2-pyridinethiol (0.8 g, Maybridge Co.) and 2-chloro-1,1,1-triethoxyethane (1.26 g) were combined in ethanol (5 mL) and heated at 90° C. in a sealed tube for 2 hours. The mixture was allowd to cool to room temperature and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by flash chromatography (2:1, dichloromethane:hexanes) to provide the title compound. 1H NMR (CDCl3, 300 MHz) δ 4.00 (3H, s), 4.88 (2H, s), 6.88 (1H, d, J=8.7 Hz), 8.10 (1H, d, J=8.7 Hz); MS (DCI/NH3) m/z 215.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235661B2
Source datasetuspto-grants-2007_06
ORD IDord-5e8b6921a7dd4cd9a974b64d68be02c7
Source noteuspto-grants-2007_06