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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289048Generated: November 3, 2026

1,1'-Carbonyldiimidazole → HCID 57040603, compound

https://huagongshe.com/reaction/2289048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactanttert-butyl (3S)-3-aminopyrrolidine-1-carboxylateHCID 854071—
Reactant1-{[(4-Nitrophenyl)methoxy]carbonyl}piperidine-2-carboxylic acidHCID 10542803—
SolventAcetonitrileHCID 6342—
ProductHCID 57040603HCID 5704060376%

Reaction Steps

To a solution of 1-(4-nitrobenzyloxycarbonyl)-2-piperidinecarboxylic acid (1.54 g) in anhydrous acetonitrile (30 ml), N,N-carbonyldiimidazole (851 mg) was added at the room temperature, followed by stirring for one hour. The reaction mixture was allowed to react with a solution of (3S)-3-amino-1-(tert-butoxycarbonyl)pyrrolidine (931 mg) in anhydrous acetonitrile (15 ml) under ice cooling in a similar manner to that described in Referential Example 1-(1), whereby 1.81 g of (3S)-1-(tert-butoxycarbonyl)-3-[1-(4-nitrobenzyloxycarbonyl)piperidin-2-ylcarbonylamino]pyrrolidine were obtained as a colorless amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090802
Source datasetuspto-grants-2000_07
ORD IDord-39a1d75dcba947949e321653cc4612ca
Source noteuspto-grants-2000_07