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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30475Generated: October 29, 2026

1-(But-3-yn-1-yl)piperidine → 2-(4-Piperidin-1-yl-but-1-ynyl)-6-piperidin-1-ylmethyl-pyridine

https://huagongshe.com/reaction/30475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(But-3-yn-1-yl)piperidineHCID 13155986—
Reactant2-Bromo-6-piperidin-1-ylmethylpyridineHCID 13784544—
Product2-(4-Piperidin-1-yl-but-1-ynyl)-6-piperidin-1-ylmethyl-pyridineHCID 11580437—

Reaction Steps

The title compound was prepared in a manner similar to that described in Example 18, Step D, using 2-bromo-6-piperidin-1-ylmethyl-pyridine and 1-but-3-ynyl-piperidine (56%). MS (ESI): exact mass calcd. for C20H29N3, 311.46; m/z found, 312.5 [M+H]+. 1H NMR (500 MHz, CDCl3): 7.54 (t, J=7.7, 1H), 7.38 (d, J=7.7, 1H), 7.20 (d, J=7.4, 1H), 3.58 (s, 2H), 2.67-2.57 (m, 4H), 2.46-2.34 (m, 8H), 1.60-1.50 (m, 8H), 1.44-1.36 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423147B2
Source datasetuspto-grants-2008_09
ORD IDord-ef144f22d0684cbdb91a628394411252
Source noteuspto-grants-2008_09