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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400714Generated: November 1, 2026

HCID 86694047, compound → HCID 86694048, compound

https://huagongshe.com/reaction/2400714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86694047HCID 86694047—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86694048HCID 8669404899.5%

Reaction Steps

To a solution of tert-butyl 4-({[(2S,5R)-6-benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)piperazine-1-carboxylate 206 (0.25 g, 0.54 mml) in methanol (15 mL) was added 10% Pd/C (0.3 g). The mixture was hydrogenated under 35 psi hydrogen atmosphere at room temperature for 2 h. The catalyst was filtered out through Celite, and the filtrate was evaporated to give tert-butyl 4-({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)piperazine-1-carboxylate 207 (0.20 g, 99%) as a colorless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796257B2
Source datasetuspto-grants-2014_08
ORD IDord-42f22a22f86c41f683ba9fae2768f252
Source noteuspto-grants-2014_08