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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465505Generated: October 26, 2026

tert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylate → tert-butyl 4-[6-(2-{5-[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]thiophen-3-yl}vinyl)pyridin-3-yl]piperazine-1-carboxylate

https://huagongshe.com/reaction/1465505

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylateHCID 58181229—
Reactant({5-[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]thiophen-3-yl}methyl)(triphenyl)phosphonium chlorideHCID 86651854—
Producttert-butyl 4-[6-(2-{5-[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]thiophen-3-yl}vinyl)pyridin-3-yl]piperazine-1-carboxylateHCID 6726714194.8%

Reaction Steps

By a method similar to Production Example 108, step 4, ({5-[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]thiophen-3-yl}methyl)(triphenyl)phosphonium chloride (1.724 g, 3.600 mmol) and tert-butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylate (874.1 mg, 3.000 mmol) were condensed to give tert-butyl 4-[6-(2-{5-[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]thiophen-3-yl}vinyl)pyridin-3-yl]piperazine-1-carboxylate (1.295 g, yield 94.7%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-09bb4f93b02842898be353e8c8a761d7
Source noteuspto-grants-2015_04