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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330974Generated: October 31, 2026

HCID 86693996, compound → HCID 86693998, compound

https://huagongshe.com/reaction/330974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86693996HCID 86693996—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86693998HCID 8669399878%

Reaction Steps

To a solution of tert-butyl 2-{[({[(2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]methyl}-1,4-oxazepane-4-carboxylate 132 (0.32 g, 0.63 mml) in methanol (20 mL) was added 5% Pd/C (0.30 g). The mixture was hydrogenated at 15 psi hydrogen atmosphere at room temperature for 1 h. The catalyst was filtered out through Celite, and the filtrate was evaporated to give tert-butyl 2-{[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]methyl}-1,4-oxazepane-4-carboxylate 133 (0.205 g, 78%) as a colorless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877743B2
Source datasetuspto-grants-2014_11
ORD IDord-b03a27ed40d24d21a4949306ab3f7b64
Source noteuspto-grants-2014_11