Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110549Generated: October 30, 2026

Pyridine, 3-(4-aminobutyl)- → (Z)-5,5-bis(3-methoxyphenyl)-N-[4-(3-pyridinyl)-butyl]-2,4-pentadienamide

https://huagongshe.com/reaction/1110549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine, 3-(4-aminobutyl)-HCID 72927—
Reactant(Z)-5,5-bis(3-methoxyphenyl)-2,4-pentadienoic acid 4-nitrophenyl esterHCID 14347313—
Reactant(E)-5,5-bis(3-nitrophenyl)-N-[4-(3-pyridinyl)butyl)-2,4-pentadienamideHCID 14347344—
SolventTetrahydrofuranHCID 8028—
Product(Z)-5,5-bis(3-methoxyphenyl)-N-[4-(3-pyridinyl)-butyl]-2,4-pentadienamideHCID 1434733539%

Reaction Steps

As in Example 134, a solution of (Z)-5,5-bis(3-methoxyphenyl)-2,4-pentadienoic acid 4-nitrophenyl ester (1.2 g) and 3-pyridinebutanamine (0.42 g) in tetrahydrofuran (7 mL) was stirred at room temperature for 1 hour. The crude amide that had been isolated in the usual way, was contaminated with a minor amount of the (E)-isomer. The mixture was separated by HPLC (ethyl acetate) and the desired product was crystallized from ether (2x) to yield 0.48 g of (Z)-5,5-bis(3-methoxyphenyl)- N-[4-(3-pyridinyl)-butyl]-2,4-pentadienamide mp 69°-73° C. Anal. Calculated for C28H30N2O3 : C, 75.99; H, 6.83; N, 6.33 Found: C, 75.79; H, 6.70; N, 6.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04975438
Source datasetuspto-grants-1990_12
ORD IDord-220143f3437d4f3a8bb1677f7f5a7e15
Source noteuspto-grants-1990_12