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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934591Generated: October 28, 2026

Benzaldehyde → HCID 22466442, compound

https://huagongshe.com/reaction/1934591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantThiopheneHCID 8030—
ReactantHCID 77776170HCID 77776170—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 22466442HCID 22466442—

Reaction Steps

A mixture of compound 37 (0.0029 mol) and benzaldehyde (0.0029 mol) in methanol (250 ml) was hydrogenated at 50° C. overnight with Pd on activated carbon 10% (2 g) as a catalyst in the presence of thiophene solution (2 ml). After uptake of hydrogen, the catalyst was filtered off and the filtrate was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 98/2). The pure fractions were collected and the solvent was evaporated. The residue was triturated in DIPE and 2-propanol, filtered off and dried, yielding 1.1 g (48%) of [2S-[2α,4α(S*,R*)]]-4-[4-[4-[4-[[2-(2,4-difluorophenyl)-2-(1H-1,2,4-triazol-1-yl-methyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-1-piperazinyl]phenyl]-2,4-dihydro-2-[2-[(phenylmethyl)amino]-1-methylpropyl]-3H-1,2,4-triazol-3-one (compound 106; mp. 154.3° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384030B1
Source datasetuspto-grants-2002_05
ORD IDord-263c9e03eb434a3f8735db6fd3c44b40
Source noteuspto-grants-2002_05