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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979203Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 86756896, compound

https://huagongshe.com/reaction/1979203

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 86756897HCID 86756897—
SolventMethanolHCID 887—
ProductHCID 86756896HCID 8675689688.8%

Reaction Steps

A solution of 2.12 g of (E)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-(2(R)-hydroxypropionyl)-2′-isobutyl-4-methylvalerohydrazide in 20 ml of methanol was treated with 0.212 g of p-toluenesulphonic acid. The mixture was stirred for 0.5 hour at room temperature and evaporated to give a foam. This foam in ethyl acetate was washed with 5% sodium hydrogen carbonate solution and water, dried over anhydrous magnesium sulphate and evaporated to low volume. The solid which separated was washed with cold ethyl acetate and dried to give 1.584 g of (E)-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenyl-3-butenyl]-2′-(2(R)-hydroxypropionyl)-2′-isobutyl-4-methylvalerohydrazide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239151B1
Source datasetuspto-grants-2001_05
ORD IDord-bdc76110ae0641909285774b352b229c
Source noteuspto-grants-2001_05