Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289046Generated: November 1, 2026

1,1'-Carbonyldiimidazole → HCID 57047864, compound

https://huagongshe.com/reaction/2289046

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactanttert-butyl (3S)-3-aminopyrrolidine-1-carboxylateHCID 854071—
ReactantHCID 53963276HCID 53963276—
SolventAcetonitrileHCID 6342—
ProductHCID 57047864HCID 5704786446.6%

Reaction Steps

To a solution of 4-hydroxy-1-(4-nitrobenzyloxycarbonyl)-L-proline (1.79 g) in anhydrous acetonitrile (30 ml), N,N,-carbonyldiimidazole (981 mg) was added at room temperature, followed by stirring at room temperature for one hour. To the reaction mixture, a solution of (3S)-3-amino-1-(tert-butoxycarbonyl)pyrrolidine (1.02 g) in anhydrous acetonitrile (20 ml) was added under ice cooling. The resulting mixture was stirred at room temperature for 6 hours. The reaction mixture was purified in a similar manner to that described in Referential Example 1-(1), whereby 1.22 g of (3S)-1-(tert-butoxycarbonyl)-3-[1-(4-nitrobenzyloxycarbonyl)-4-hydroxy-L-prolylamino]pyrrolidine were obtained as an amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090802
Source datasetuspto-grants-2000_07
ORD IDord-c7f67cc635d448bb84834a6142fe793a
Source noteuspto-grants-2000_07