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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247940Generated: October 31, 2026

Hydrochloric Acid → 4,5,6,7-Tetrahydrothiazolo[5,4-c]pyridin-2(1H)-one

https://huagongshe.com/reaction/2247940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium thiocyanateHCID 15666—
Reactant1-Acetyl-3-bromopiperidin-4-one hydrobromideHCID 19761176—
ReactantN-acetyl-3-thiocyanato-4-piperidoneHCID 19816092—
SolventWaterHCID 962—
Product4,5,6,7-Tetrahydrothiazolo[5,4-c]pyridin-2(1H)-oneHCID 144238776%

Reaction Steps

Ammonium thiocyanate (5.54 g, 72.8 mmol) was mixed with water (450 ml) and heated to 80°. A solution of N-acetyl-3-bromo-4-piperidone hydrobromide (20.0 g, 66.2 mmol) in water (200 ml) was added dropwise over 3 hours. The reaction was then allowed to stir at 80° for sixteen hours. The reaction solution (containing the crude N-acetyl-3-thiocyanato-4-piperidone) was treated with concentrated hydrochloric acid (6 ml of a 12M solution, 93 mmol) and heated to reflux for 2 hours. The reaction mixture was then freeze-dried, and the residue dissolved in methanol and filtered. The precipitate was purified by column chromatography (eluant: 89:10:1 chloroform:methanol: concentrated ammonium hydroxide) to provide the title product as a white solid, m.p. 208° (decomp.) (0.60 g, 3.8 mmol, 6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037834
Source datasetuspto-grants-1991_08
ORD IDord-39d6f679d89a4baaaf5bcd61f1893f3d
Source noteuspto-grants-1991_08