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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55303Generated: October 26, 2026

N-benzenesulfonyl-4-ethinylbenzoic acid amide → 3-{3-[6-(4-methoxyphenyl)-(5E)-5-hexenyloxy]-6-[2-(4-benzenesulfonamidocarbonylphenyl)-ethinyl]-2-pyridyl}-propionic acid methyl ester

https://huagongshe.com/reaction/55303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-benzenesulfonyl-4-ethinylbenzoic acid amideHCID 54259246—
Reactant3-{6-iodo-3-[6-(4-methoxyphenyl)-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl esterHCID 86750763—
Product3-{3-[6-(4-methoxyphenyl)-(5E)-5-hexenyloxy]-6-[2-(4-benzenesulfonamidocarbonylphenyl)-ethinyl]-2-pyridyl}-propionic acid methyl esterHCID 6770372030%

Reaction Steps

Under the conditions of example 5 A, 1.31 g of the crude N-benzenesulfonyl-4-ethinylbenzoic acid amide is reacted with 1.9 g of 3-{6-iodo-3-[6-(4-methoxyphenyl)-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl ester, worked up, and the crude product is chromatographed on silica gel with dichloromethane/0-5% methanol. 750 mg of 3-{3-[6-(4-methoxyphenyl)-(5E)-5-hexenyloxy]-6-[2-(4-benzenesulfonamidocarbonylphenyl)-ethinyl]-2-pyridyl}-propionic acid methyl ester is obtained as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624943
Source datasetuspto-grants-1997_04
ORD IDord-beb9ae21e7e7406597b47c3add4334d1
Source noteuspto-grants-1997_04