Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400621Generated: October 28, 2026

HCID 86693941, compound → HCID 86693942, compound

https://huagongshe.com/reaction/2400621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86693941HCID 86693941—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86693942HCID 8669394291.9%

Reaction Steps

To a solution of tert-butyl 3-[({[(2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]azetidine-1-carboxylate 37 (0.15 g, 0.34 mml) in methanol (15 mL) was added 5% Pd/C (0.3 g). The mixture was hydrogenated under 35 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 3-[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]azetidine-1-carboxylate 38 (0.11 g, 91%) as a colorless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796257B2
Source datasetuspto-grants-2014_08
ORD IDord-c99f2132d82e4767bc23e25722f4367c
Source noteuspto-grants-2014_08