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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979243Generated: October 29, 2026

p-Toluenesulfonic acid monohydrate → HCID 86756952, compound

https://huagongshe.com/reaction/1979243

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 86756954HCID 86756954—
SolventMethanolHCID 887—
ProductHCID 86756952HCID 8675695271.5%

Reaction Steps

A solution of 0.390 g of 2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenylbutyl]-2′-[2-(1-imidazoyl)acetyl]-2′-isobutyl-4-methylvalerohydrazide in 5 ml of methanol was treated with 0.143 g of p-toluenesulphonic acid monohydrate. The mixture was stirred at room temperature for 1 hour and evaporated. The residue was triturated with diethyl ether, filtered and dried to give 0.320 g of 2(R)-[1(S)-(hydroxycarbamoyl)-4-phenylbutyl]-2′-[2-(1-imidazoyl)acetyl]-2′-isobutyl-4-methylvalerohydrazide p-toluenesulphonate in the form of a pale pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239151B1
Source datasetuspto-grants-2001_05
ORD IDord-ed86e3206db54717ab92dc1ede3854b6
Source noteuspto-grants-2001_05