Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337216Generated: October 26, 2026

Diisopropylethylamine → 4-(4-tert-Butoxycarbonylamino-piperidine-1-sulfonyl)-2-fluoro-benzoic acid methyl ester

https://huagongshe.com/reaction/337216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantMethyl 4-(chlorosulfonyl)-2-fluorobenzoateHCID 57732146—
SolventDichloromethaneHCID 6344—
Product4-(4-tert-Butoxycarbonylamino-piperidine-1-sulfonyl)-2-fluoro-benzoic acid methyl esterHCID 7106026694.1%

Reaction Steps

Diisopropylethylamine (3.2 ml, 18.5 mmol) was added in one portion to a stirred solution of piperidin-4-yl-carbamic acid tert-butyl ester (0.5 g, 2.5 mmol) in DCM (10 ml) at room temperature. To this mixture was added 4-chlorosulfonyl-2-fluoro-benzoic acid methyl ester (0.6 g, 2.5 mmol) in one portion and the mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour. After this time the mixture was diluted with DCM (50 ml) and washed sequentially with HCl (1M solution, 10 ml), NaOH (1M solution, 10 ml) and brine (10 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated. The resulting residue was purified by flash column chromatography (elution: 98% DCM, 2% Methanol) to give the title compound (0.98 g, 87% yield) as a white solid. Tr=2.08 min m/z (ES+) (M+Na+) 439.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889716B2
Source datasetuspto-grants-2014_11
ORD IDord-8038d215d4ae41dca06eaade5d338aea
Source noteuspto-grants-2014_11