Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717963Generated: October 26, 2026

Ammonium Hydroxide → Ethyl 2-(piperidin-4-yl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/717963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 3-ethoxy-2-propenoateHCID 221780—
Reactanttert-Butyl 4-carbamothioylpiperidine-1-carboxylateHCID 2735648—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductEthyl 2-(piperidin-4-yl)-1,3-thiazole-5-carboxylateHCID 86701983—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Ethyl 3-ethoxyacrylate (1.50 g, 10.38 mml) was dissolved in dioxane/water and chilled to −10° C. N-Bromosuccinimide (2.03 g, 11.42 mmol) was added and the mixture was stirred 1 hour at room temperature. tert-Butyl 4-carbamothioylpiperidine-1-carboxylate (2.54 g, 10.38 mmol) was added and the mixture was heated at 100° C. for 1 hour. The reaction mixture was poured into 25 mL saturated ammonium hydroxide and extracted with dichloromethane. The combined organic layers were washed with brine, dried with sodium sulfate, filtered, and concentrated. Normal phase chromatography provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193723B2
Source datasetuspto-grants-2015_11
ORD IDord-ea33df414eef4f0ab07f324266e29870
Source noteuspto-grants-2015_11