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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353511Generated: October 30, 2026

Bis-(2-chloro-ethyl)-(4-methoxy-benzyl)-amine → 4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/353511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis-(2-chloro-ethyl)-(4-methoxy-benzyl)-amineHCID 415290—
ReactantEthyl{[4-(2-butynyloxy)phenyl]sulfonyl}acetateHCID 11335441—
Product4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperidine-4-carboxylic acid ethyl esterHCID 11363756—

Reaction Steps

4-(4-but-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperidine-4-carboxylic acid ethyl ester was prepared according to the general method as outlined in Example 1. Starting from (4-but-2-ynyloxy-benzenesulfonyl)-acetic acid ethyl ester (2 g, 6.73 mmol) and bis-(2-chloro-ethyl)-(4-methoxy-benzyl)-amine (2.61 g, 8.75 mmol) and following the procedure as outlined in Example 1 (Step 6) 2.5 g of the product was isolated. Yield 2.5 g (77%); yellow oil; MS: 486 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753337B2
Source datasetuspto-grants-2004_06
ORD IDord-16fbafb10611453d85bd73db29f4c9dc
Source noteuspto-grants-2004_06