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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278302Generated: October 29, 2026

Benzenemethanamine, N,N-bis(2-chloroethyl)-4-fluoro- → 4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-fluoro-benzyl)-piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/278302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenemethanamine, N,N-bis(2-chloroethyl)-4-fluoro-HCID 15240—
ReactantEthyl{[4-(2-butynyloxy)phenyl]sulfonyl}acetateHCID 11335441—
Product4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-fluoro-benzyl)-piperidine-4-carboxylic acid ethyl esterHCID 54562587—

Reaction Steps

4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-fluoro-benzyl)-piperidine-4-carboxylic acid ethyl ester 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 (5 g, 16.9 mmol) and (4-fluoro-benzyl)-bis-(2-chloro-ethyl)-amine (5.8 g, 20.1 mmol) 5.3 g of the product was isolated. Yield 5.3 g (67%); Brown oil; MS: 474 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358980B1
Source datasetuspto-grants-2002_03
ORD IDord-148f13eb8d614716978e5477098d3afa
Source noteuspto-grants-2002_03