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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454418Generated: October 30, 2026

HCID 178502361, compound → HCID 178502363, compound

https://huagongshe.com/reaction/454418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178502361HCID 178502361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 178502363HCID 178502363—

Reaction Steps

Phenylmethyl (3S)-3-(4-{4′-[2-((2S)-1-{N-[(methyloxy)carbonyl]-L-valyl}-2-pyrrolidinyl)-1H-imidazol-4-yl]-4-biphenylyl}-1H-imidazol-2-yl)-6,10-dioxa-2-azaspiro[4.5]decane-2-carboxylate (Intermediate 22) (1.44 g, 1.83 mmol) was hydrogenated in ethanol (100 mL) with balloon under the catalysis of Pd/C for 20 hrs to give methyl [(1S)-1-({(2S)-2-[4-(4′-{2-[(3S)-6,10-dioxa-2-azaspiro[4.5]dec-3-yl]-1H-imidazol-4-yl}-4-biphenylyl)-1H-imidazol-2-yl]-1-pyrrolidinyl}carbonyl)-2-methylpropyl]carbamate (Intermediate 19). ES LC-MS m/z=654.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492554B2
Source datasetuspto-grants-2013_07
ORD IDord-59f1e816056a467eb615461c892a0808
Source noteuspto-grants-2013_07