Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20550Generated: October 28, 2026

tert-butyl 3-({3-(benzyloxy)-5-[(1S)-2-methoxy-1-methylethoxy]benzoyl}amino)-1H-pyrazole-1-carboxylate → tert-Butyl 3-({3-hydroxy-5-[(1S)-2-methoxy-1-methylethoxy]benzoyl}amino)-1H-pyrazole-1-carboxylate

https://huagongshe.com/reaction/20550

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 3-({3-(benzyloxy)-5-[(1S)-2-methoxy-1-methylethoxy]benzoyl}amino)-1H-pyrazole-1-carboxylateHCID 59127136—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3-({3-hydroxy-5-[(1S)-2-methoxy-1-methylethoxy]benzoyl}amino)-1H-pyrazole-1-carboxylateHCID 5912718597%

Reaction Steps

A solution of tert-butyl 3-({3-(benzyloxy)-5-[(1S)-2-methoxy-1-methylethoxy]benzoyl}amino)-1H-pyrazole-1-carboxylate (23 g, 47.8 mmol) in THF (140 mL) and ethanol (140 mL) was evacuated and purged with nitrogen (×3). 10% Palladium on carbon (2.3 g, 10% w/w) was added and reaction mixture was evacuated and finally purged with hydrogen gas. Reaction mixture was left to stir at ambient temperature under a hydrogen balloon for 16-hours. Pd/C was filtered through diatomaceous earth and the filtrate concentrated in vacuo to give a white, foam (18 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745475B2
Source datasetuspto-grants-2010_06
ORD IDord-8bf7d6cee8114df88f7824bf2a2e6cf1
Source noteuspto-grants-2010_06