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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265861Generated: October 26, 2026

Triethylamine → 3-[2-(N-Boc-Piperidin-4-yl)ethylaminosulfonyl]benzoic Acid

https://huagongshe.com/reaction/265861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzoic acid, 3-(chlorosulfonyl)-HCID 77641—
Reactanttert-Butyl 4-(2-aminoethyl)piperidine-1-carboxylateHCID 1514258—
SolventChloroformHCID 6212—
Product3-[2-(N-Boc-Piperidin-4-yl)ethylaminosulfonyl]benzoic AcidHCID 19034162—

Reaction Steps

A solution of 2-(N-Boc-4-piperidinyl)ethyl-amine (1-6) (0.45 g, 2.0 mmoles) in CHCl3 (20 ml) was treated with added triethylamine (0.405 g, 4.0 mmoles) followed by 3-chlorosulfonylbenzoyl chloride (3-1) (0.44 g, 2.0 mmoles) and the resulting solution was stirred at room temperature for 16 hours. The solvent was then removed and the residue was taken up in EtOAc and washed with H2O, 10% KHSO4 solution, brine and dried (Na2SO4). Solvent removal provided a residue that was purified by flash chromatography on silica gel eluting with CHCl3 (95)/MeOH(5) to give pure 4-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648368
Source datasetuspto-grants-1997_07
ORD IDord-b8cfed57af6547d7841db1e7028c3020
Source noteuspto-grants-1997_07