Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593018Generated: November 3, 2026

2-(4-Chlorophenyl)ethanethioamide → HCID 69448752, compound

https://huagongshe.com/reaction/1593018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Chlorophenyl)ethanethioamideHCID 2734827—
ReactantProp-2-en-1-yl 4-(bromoacetyl)piperidine-1-carboxylateHCID 18623152—
SolventEthanolHCID 702—
ProductHCID 69448752HCID 69448752—

Reaction Steps

A mixture of allyl 4-(bromoacetyl)piperidine-1-carboxylate (547 mg) and 2-(4-chlorophenyl)ethanethioamide (366 mg) in ethanol (15 ml) was refluxed for 5 hours. The reaction mixture was evaporated to dryness and the residue was purified by chromatography on silica eluting with methanol/dichloromethane (2:98) to give allyl 4-[2-(4-chlorobenzyl)-1,3-thiazol-4-yl]piperidine-1-carboxylate. Yield 698 mg. NMR (CDCl3): 1.65 (m, 2H), 2.25 (m, 2H), 2.95 (m, 2H), 3.2 (m, 1H), 4.3 (m, 2H), 4.55 (m, 4H), 5.3 (m, 2H), 6.0 (m, 1H), 6.95 (s, 1H), 7.35 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294636B2
Source datasetuspto-grants-2007_11
ORD IDord-09d090415d694169962be4fb7eaf3062
Source noteuspto-grants-2007_11