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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794068Generated: October 27, 2026

Water → HCID 86585992, compound

https://huagongshe.com/reaction/1794068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTert-butyl 4-(chlorocarbonyl)piperazine-1-carboxylateHCID 11334154—
Reactant4-(4-Fluoro-benzyloxy)-phenyl-methanethiolHCID 22219894—
SolventPyridineHCID 1049—
ProductHCID 86585992HCID 8658599245.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

5.84 g (23.5 mmol) 4-chlorocarbonyl-piperazine-1-carboxylic acid tert-butyl ester were added to a solution of 6.0 g (24.2 mmol) 4-(4-fluoro-benzyloxy)-phenyl-methanethiol in 14.6 ml pyridine. The solution was heated to 100° C. for 3.5 h, then cooled to rt, 10 ml of water added and the volume reduced to a third. The resulting precipitate is collected, washed with water and dried. The crude product is re-crystallized from hexane/AcOEt. Flash chromatography on silica gel provided 4.90 g 4-[4-(4-fluoro-benzyloxy)-benzylsulfanylcarbonyl]-piperazine-1-carboxylic acid tert-butyl ester as colourless powder, mp: 123–124° C. 1H-NMR (CDCl3): 1.46 s, 9H; 3.38–3.60 m, 8H; 4.13 s, 2H; 5.00 s, 2H; 6.89 d, 2H, 7.06 t, 2H, 7.28 d, 2H and 7.40 dd, 2H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022707B2
Source datasetuspto-grants-2006_04
ORD IDord-72ce5e97c5474011a688e9ecae84b0ae
Source noteuspto-grants-2006_04