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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451302Generated: October 30, 2026

tert-Butyl (4S)-4-({[(2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)azepane-1-carboxylate → tert-Butyl (4S)-4-({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)azepane-1-carboxylate

https://huagongshe.com/reaction/451302

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (4S)-4-({[(2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)azepane-1-carboxylateHCID 86659585—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl (4S)-4-({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)azepane-1-carboxylateHCID 8665958635.5%

Reaction Steps

Palladium on carbon (11.8 mg; 10% Pd/C) was added to a solution of tert-butyl (4S)-4-({[(2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)azepane-1-carboxylate (49.7 mg, 0.33 mmol) in methanol (1.5 mL) and the resulting mixture was stirred under hydrogen (balloon) for 3 hours. TLC analysis showed the reaction was complete. The reaction mixture was filtered through a microfilter and the filtrate was concentrated under vacuum to afford the impure title compound as a white foam (44.8 mg) which was used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487093B2
Source datasetuspto-grants-2013_07
ORD IDord-3ff4fb84f79946acb5d90fd129fe6fb3
Source noteuspto-grants-2013_07