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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244485Generated: October 31, 2026

HCID 15389740, compound → HCID 178440877, compound

https://huagongshe.com/reaction/1244485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15389740HCID 15389740—
ReactantHCID 86584206HCID 86584206—
ReactantHCID 178441077HCID 178441077—
ProductHCID 178440877HCID 17844087762%

Reaction Steps

The experimental protocol used is the same as that described for compound 1, with 3-[(3,5-bis-(1,1-dimethylethyl)-4-hydroxyphenyl]-N-(4-hydroxy-3-aminophenyl)-2-propenamide replacing the 3,5-bis-(1,1-dimethylethyl)4-hydroxy-N-(4-aminophenyl)-benzamide. The free base is purified on a silica column (eluant: heptane/ethyl acetate: 35/65). The pure fractions are collected and concentrated under reduced pressure. The evaporation residue is diluted in 10 ml of acetone and salified with a molar solution of HCl in anhydrous ether, as described previously. 0.35 g (62%) of a yellow powder is obtained. Melting point: 199-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122535B2
Source datasetuspto-grants-2006_10
ORD IDord-eade439e8e75427ea98420baf4adf86e
Source noteuspto-grants-2006_10