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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071012Generated: October 30, 2026

({2-[({(3S,7R,8R,9S)-7-benzyl-9-methyl-8-[(2-methylprop-2-enyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}amino)carbonyl]-4-methoxypyridine-3-yl}oxy)methyl acetate → {[2-({[(3S,7R,8R,9S)-7-benzyl-8-isobutoxy-9-methyl-2,6-dioxo-1,5-dioxonan-3-yl}amino)carbonyl]-4-methoxypyridine-3-yl}oxy)methyl acetate

https://huagongshe.com/reaction/1071012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant({2-[({(3S,7R,8R,9S)-7-benzyl-9-methyl-8-[(2-methylprop-2-enyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}amino)carbonyl]-4-methoxypyridine-3-yl}oxy)methyl acetateHCID 59989553—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product{[2-({[(3S,7R,8R,9S)-7-benzyl-8-isobutoxy-9-methyl-2,6-dioxo-1,5-dioxonan-3-yl}amino)carbonyl]-4-methoxypyridine-3-yl}oxy)methyl acetateHCID 5998958195%

Reaction Steps

Compound 12 was prepared in 95% yield using Compound 6 (6.0 g, 10.5 mmol) with 10% palladium on charcoal (1.2 g) and hydrogen (40 psi) in ethyl acetate (150 mL) for 1.5 hour. Recrystallization from a mixture of hot methylcyclohexane and toluene (4:1) gave 5.7 g of white needles: m.p.134-136° C. Spectral data were consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903219B2
Source datasetuspto-grants-2005_06
ORD IDord-d6168b821f794d7d803151779a3c1c72
Source noteuspto-grants-2005_06