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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038555Generated: November 1, 2026

HCID 59547335, compound → HCID 59547341, compound

https://huagongshe.com/reaction/2038555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59547335HCID 59547335—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59547341HCID 59547341—

Reaction Steps

Palladium (10%) on carbon (100 mg) was wetted with MeOH (2.5 mL) and added to (5S,8S)-tert-butyl 7-((S)-2-(benzyloxycarbonylamino)-3,3-dimethylbutanoyl)-2-oxo-3-phenyl-1-oxa-3,7-diazaspiro[4.4]nonane-8-carboxylate (E1) (323 mg, 411 mot, 1 eq.). The reaction was hydrogenated at 50 psi overnight at room temp., then filtered and concentrated to give (5S,8S)-tert-butyl 7-((S)-2-amino-3,3-dimethylbutanoyl)-2-oxo-3-phenyl-1-oxa-3,7-diazaspiro[4.4]nonane-8-carboxylate (F1) in quantitative yield. LC MS+: 432.39 at 1.94 min (10-90%, 3-5 min, Formic Acid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575208B2
Source datasetuspto-grants-2013_11
ORD IDord-a2eb16fb08eb4db9a9002106efae6806
Source noteuspto-grants-2013_11