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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241427Generated: November 1, 2026

Triethylamine → Tert-butyl 4-(1,1-dioxidothietan-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1241427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Chloro-1lambda6-thietane-1,1-dioneHCID 265636—
Reactanttert-Butyl 4-(6-aminopyrimidin-4-yl)piperazine-1-carboxylateHCID 21934614—
Solvent1-ButanolHCID 263—
ProductTert-butyl 4-(1,1-dioxidothietan-3-yl)piperazine-1-carboxylateHCID 21060000—

Reaction Conditions

Temperature150 °C

Reaction Steps

3-Chlorothietane 1,1-dioxide 50-1 (0.50 g, 3.56 mmol) was dissolved in n-butanol (4 mL) then triethylamine (1.08 g, 10.67 mmol) was added followed by tert-butyl piperazine-1-carboxylate 12-1 (0.66 g, 3.56 mmol). This was then stirred at 150° C. for 5 hours. Upon cooling the solid was filtered off, washed with n-butanol, ethyl ether and then purified on a silica column to afford 50-2. 1H-NMR (CDCl3): 4.10(complex, 4H); 3.46(t, 4H); 3.19(m, 1H); 2.36(t, 4H); 1.46(s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115597B2
Source datasetuspto-grants-2006_10
ORD IDord-f82d0040d320477bad82445d9a6cd128
Source noteuspto-grants-2006_10