Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636056Generated: October 30, 2026

L-Malic Acid → HCID 131722769, compound

https://huagongshe.com/reaction/1636056

Reaction equation

Participants

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

Reaction Steps

[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 (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 numberUS06512116B2
Source datasetuspto-grants-2003_01
ORD IDord-28b1b24888ab4ba4b9805f91c7883df0
Source noteuspto-grants-2003_01