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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353541Generated: October 30, 2026

Ethyl{[4-(2-butynyloxy)phenyl]sulfonyl}acetate → Ethyl 4-([4-(2-butynyloxy)phenyl]sulfonyl)-1-(3-pyridinylmethyl)-4-piperidine carboxylate

https://huagongshe.com/reaction/353541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl{[4-(2-butynyloxy)phenyl]sulfonyl}acetateHCID 11335441—
Reactant3-Pyridyl methyl[bis(2-chloroethyl)]amine hydrochlorideHCID 69886982—
ProductEthyl 4-([4-(2-butynyloxy)phenyl]sulfonyl)-1-(3-pyridinylmethyl)-4-piperidine carboxylateHCID 235138425%

Reaction Steps

Ethyl 4-{[4-(2-butynyloxy)phenyl]sulfonyl}-1-(3-pyridinylmethyl)-4-piperidine carboxylate was prepared according to the general method as outlined in example 1 (step 6), starting from (4-but-2-ynyloxy-benzenesulfonyl)-acetic acid ethyl ester (4 g, 16.9 mmol) and 3-pyridyl methyl [bis(2-chloroethyl)]amine hydrochloride (4.18 g, 18.6 mmol); 370 mg brown oil. Yield 5%; MS: 457.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753337B2
Source datasetuspto-grants-2004_06
ORD IDord-664a34b91d1f4b0582d20539012b182c
Source noteuspto-grants-2004_06