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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979190Generated: October 30, 2026

p-Toluenesulfonic acid → (E)-2'-[(1-amino-1-cyclopentyl)carbonyl]-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenyl-3-butenyl]-2'-isobutyl-4-methylvalerohydrazide p-toluenesulphonate

https://huagongshe.com/reaction/1979190

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant(E)-2'-[(1-amino-1-cyclopentyl)carbonyl]-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2'-isobutyl-4-methylvalerohydrazideHCID 86756877—
SolventMethanolHCID 887—
Product(E)-2'-[(1-amino-1-cyclopentyl)carbonyl]-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenyl-3-butenyl]-2'-isobutyl-4-methylvalerohydrazide p-toluenesulphonateHCID 8675687579.2%

Reaction Steps

A solution of 0.35 g of (E)-2′-[(1-amino-1-cyclopentyl)carbonyl]-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]4-phenyl-3-butenyl]-2′-isobutyl-4-methylvalerohydrazide in 3 ml of methanol was treated with 0.14 g of p-toluenesulphonic acid. The mixture was stirred for 1.7 hours at room temperature and evaporated to give a foam. This foam was triturated with diethyl ether, filtered off and dried to give 0.32 g of (E)-2′-[(1-amino-1-cyclopentyl)carbonyl]-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenyl-3-butenyl]-2′-isobutyl-4-methylvalerohydrazide p-toluenesulphonate in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239151B1
Source datasetuspto-grants-2001_05
ORD IDord-741a6ff9dc6247ee8c6ea4f2b957a445
Source noteuspto-grants-2001_05