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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355606Generated: November 2, 2026

4-Methoxy-3-(2-methylpropoxy)benzaldehyde → 6-[1-(3-Isobutoxy-4-methoxy-benzyl)-piperidin-4-ylamino]-4-trifluoromethyl-nicotinamide

https://huagongshe.com/reaction/2355606

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-3-(2-methylpropoxy)benzaldehydeHCID 2414110—
Reactant6-(Piperidin-4-ylamino)-4-trifluoromethyl-nicotinic acid methyl ester dihydrochlorideHCID 42604213—
Reactant6-[1-(4-Methoxy-3-propoxy-benzyl)-piperidin-4-ylamino]-4-trifluoromethyl-nicotinamideHCID 42604959—
Product6-[1-(3-Isobutoxy-4-methoxy-benzyl)-piperidin-4-ylamino]-4-trifluoromethyl-nicotinamideHCID 67400949—

Reaction Steps

The title compound was prepared in analogy to the synthesis of 6-[1-(4-methoxy-3-propoxy-benzyl)-piperidin-4-ylamino]-4-trifluoromethyl-nicotinamide (example 197) from 6-(piperidin-4-ylamino)-4-trifluoromethyl-nicotinic acid methyl ester dihydrochloride (intermediate B7) and 3-isobutoxy-4-methoxy-benzaldehyde (intermediate E12) in a yield of 15.1 mg (21%). MS (ISP): 482.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754744B2
Source datasetuspto-grants-2010_07
ORD IDord-26efb0d8ac6247e0aa6586d2cf439182
Source noteuspto-grants-2010_07