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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465486Generated: October 26, 2026

tert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylate → Tert-butyl 4-(6-{2-[4-(ethoxycarbonyl)-2-fluorophenyl]vinyl}pyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1465486

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylateHCID 58181229—
Reactant[4-(Ethoxycarbonyl)-2-fluorobenzyl](triphenyl)phosphonium bromideHCID 86651846—
ProductTert-butyl 4-(6-{2-[4-(ethoxycarbonyl)-2-fluorophenyl]vinyl}pyridin-3-yl)piperazine-1-carboxylateHCID 6703063198.9%

Reaction Steps

By a method similar to Production Example 108, step 4, [4-(ethoxycarbonyl)-2-fluorobenzyl](triphenyl)phosphonium bromide (2.513 g, 4.802 mmol) and tert-butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylate (1.166 g, 4.002 mmol) were condensed to give tert-butyl 4-(6-{2-[4-(ethoxycarbonyl)-2-fluorophenyl]vinyl}pyridin-3-yl)piperazine-1-carboxylate (1.802 g, yield 98.9%, E/Z mixture) as a pale-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-1d6eec26c38443e490b3f0c632484e19
Source noteuspto-grants-2015_04