Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26120Generated: November 1, 2026

2-Naphthalenecarboxamide, 4-amino-N-[4-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyl]-1-hydroxy- → 4-(3-Amino-4-hydroxybenzenesulfonamido)-1-hydroxy-N-[4-(2,4-di-tert-pentylphenoxy)butyl]-2-naphthamide

https://huagongshe.com/reaction/26120

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Naphthalenecarboxamide, 4-amino-N-[4-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyl]-1-hydroxy-HCID 3084862—
Reactant4-Hydroxy-3-nitrobenzene-1-sulfonyl chlorideHCID 3670479—
Product4-(3-Amino-4-hydroxybenzenesulfonamido)-1-hydroxy-N-[4-(2,4-di-tert-pentylphenoxy)butyl]-2-naphthamideHCID 23336109—

Reaction Steps

This compound was prepared in two steps by conventional procedures of the type well known in the art. 4-Amino-1-hydroxy-N-[4-(2,4-di-tert-pentylphenoxy)butyl]-2-naphthamide (U.S. Pat. No. 3,954,476, column 25) was converted to the sulfonamide by reaction with 4-hydroxy-3-nitrobenzenesulfonyl chloride. Secondly, the nitro group was reduced to the amino compound by catalytic hydrogenation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04148642
Source datasetuspto-grants-1979_04
ORD IDord-67d9671ec7044b109dcf3714e4963487
Source noteuspto-grants-1979_04