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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857166Generated: October 28, 2026

Nitrogen → tert-Butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate hydrochloride

https://huagongshe.com/reaction/857166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant(3AS,6AR)-Tert-butyl 5-benzyl-hexahydropyrrolo[3,4-C]pyrrole-2(1H)-carboxylate hclHCID 69662689—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate hydrochlorideHCID 2186762887%

Reaction Steps

To a solution of 3-benzyl-7-(tert-butoxycarbonyl)-3,7-diazabicyclo[3.3.0]-octane hydrochloride (91.1 g, 269 mmol; from step (d) above) in methanol (250 mL) under a N2 atmosphere there was added 10% Pd/C (w/w; 9.8 g). The N2 atmosphere was exchanged for H2 (1 atm of pressure) and the reaction was stirred for 18 h. The reaction was filtered through a pad of cellulose to remove the catalyst. The filtrate was concentrated in vacuo to afford an off-white solid. The solid was slurried in EtOAc and collected. After drying in a vacuum oven for 18 h at 60° C./66.5 Pa (0.5 mm Hg) there was obtained 58.0 g (87%) of the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144914B2
Source datasetuspto-grants-2006_12
ORD IDord-7b5dcdce41244360891ae62f59457790
Source noteuspto-grants-2006_12