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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972149Generated: October 29, 2026

Thiourea → 1-(4-(2-Aminothiazol-4-yl)piperidin-1-yl)ethanone

https://huagongshe.com/reaction/1972149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
Reactant1-(1-Acetylpiperidin-4-yl)-2-bromoethan-1-oneHCID 77230326—
SolventEthanolHCID 702—
Product1-(4-(2-Aminothiazol-4-yl)piperidin-1-yl)ethanoneHCID 5961003674.3%

Reaction Steps

1-(1-acetylpiperidin-4-yl)-2-bromoethanone (2.37 g, 9.561 mmol) and thiourea (0.728 g, 9.561 mmol) were dissolved in ethanol (40 mL) and agitated at ambient temperature for 30 minutes. The mixture was heated to 80° C. and agitated an additional 1 hour. Upon cooling solvent was evaporated and the residue was distributed between 20 mL of 2M NaOH and 20 mL of chloroform. The organic phase was separated and discarded. The remaining aqueous phase (white slurry) was extracted with chloroform until all solids were extracted (4×200 mL). The organic extracts were combined, dried over magnesium sulfate and evaporated to give the desired product (1.600 g, 74.27% yield) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431713B2
Source datasetuspto-grants-2013_04
ORD IDord-94f0b3db26cd45f5b0ceaf72c754f0b2
Source noteuspto-grants-2013_04