Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384877Generated: November 1, 2026

L-Malic Acid → HCID 131722769, compound

https://huagongshe.com/reaction/1384877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Malic AcidHCID 222656—
ReactantHCID 131722770HCID 131722770—
SolventEthanolHCID 702—
ProductHCID 131722769HCID 131722769—

Reaction Steps

[2S-[2α,4[(R*,R*)]]]-2-[4-[4-[4-[4-[[2-(2,4-difluorophenyl)-2-(1H-1,2,4-triazol-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-1-piperazinyl]phenyl]-4,5-dihydro-5-oxo-1H-1,2,4-triazol-1-yl]-1-methylpropyl β-alanine (0.0028 mol) was dissolved in warm ethanol (25 ml). (−)-(S)-hydroxybutanedioic acid (0.0061 mol) was added and the mixture was parboiled until complete dissolution. The resulting clear solution was allowed to cool to room temperature and the solvent was evaporated. The residue was stirred in 2-propanone, filtered off, then dried, yielding 1.53 g (53%) [2S-[2α,4α-[(R*,R*)]]]-2-[4-[4-[4-[4-[[2-(2,4-difluorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-1-piperazinyl]phenyl]-4,5-dihydro-5-oxo-1H-1,2,4-triazol-1-yl]-1-methylpropyl β-alanine (S)-hydroxybutanedioate(1:2) monohydrate (compound 12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262052B1
Source datasetuspto-grants-2001_07
ORD IDord-16ea15d8432646efa42c4be806df6d2b
Source noteuspto-grants-2001_07