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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265926Generated: November 2, 2026

2-Pyridinecarboxaldehyde → HCID 22223215, compound

https://huagongshe.com/reaction/2265926

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridinecarboxaldehydeHCID 14273—
ReactantHCID 68782917HCID 68782917—
ProductHCID 22223215HCID 22223215—
ProductHCID 68782917HCID 68782917—

Reaction Steps

The Scheme 3 shows a proposed process for synthesizing pyridinyl acrylic amide (16) with t-butyl group. Substituted pyridinecarboxaldehyde with t-butyl group (12) is prepared by reduction followed by radical substitution method (J. Heterocyclic Chem., 1989, 25, 45-48). Substituted nicotinic ester (10) is converted to corresponding pyridine-3-methanol (11). Pyridinyl-3-methanol is reacted with pivalic acid and silver nitrate to give pyridinecarboxaldehyde (12) via Tada's radical substitution. Compound (14) is synthesized from compound (12) with similar method of scheme 2. 4-t-Butylpyridinyl acrylic acid (14) is reacted with compound (15) to yield compound (16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858621B2
Source datasetuspto-grants-2010_12
ORD IDord-632d5f507cd4487daa0a2fa48d87ef41
Source noteuspto-grants-2010_12