Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804598Generated: October 31, 2026

Methanethioamide → Tert-butyl 4-(1,3-thiazol-4-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1804598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethioamideHCID 3005587—
Reactanttert-Butyl 4-(2-Bromoacetyl)piperidine-1-carboxylateHCID 18187487—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(1,3-thiazol-4-yl)piperidine-1-carboxylateHCID 5348522863%

Reaction Conditions

Temperature60 °C

Reaction Steps

The title compound from Step B above (500 mg, 1.63 mmol) was combined with thioformamide (100 mg, 1.63 mmol) in 5 mL of THF, warmed to 60° C., and stirred overnight. The mixture was cooled to RT and diluted with ethyl acetate. The solution was then washed with water followed by brine. The organics were dried over magnesium sulfate, filtered and concentrated under vacuum. Purification via preparative TLC plates (3×1000 μM) eluting with 60% ethyl acetate/hexane afforded the title compound (282 mg, 63%) as a clear oil. ESI-MS calculated for C13H20N2O2S: Exact Mass: 268.12. Found: 169.12 (M-Boc)+ and 291.14 (MNa)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354403B2
Source datasetuspto-grants-2013_01
ORD IDord-ea6c954d703d44fea793abfa1aa76855
Source noteuspto-grants-2013_01