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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289049Generated: October 30, 2026

1,1'-Carbonyldiimidazole → HCID 54375516, compound

https://huagongshe.com/reaction/2289049

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantTert-butyl 3-aminoazetidine-1-carboxylateHCID 1516507—
ReactantHCID 53836194HCID 53836194—
SolventAcetonitrileHCID 6342—
ProductHCID 54375516HCID 5437551680.3%

Reaction Steps

To a solution of 1-(4-nitrobenzyloxycarbonyl)-L-proline (2.81 g) in anhydrous acetonitrile (40 ml), N,N-carbonyldiimidazole (1.42 g) was added at room temperature, followed by stirring for one hour. The reaction mixture was allowed to react under ice cooling with a solution of 3-amino-1-(tert-butoxycarbonyl)azetidine (1.31 g) in anhydrous acetonitrile (10 ml) in a similar manner to that described in Referential Example 1-(1), whereby 2.74 g of 1-(tert-butoxycarbonyl)-3-[1-(4-nitrobenzyloxycarbonyl)-L-prolylamino]azetidine were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090802
Source datasetuspto-grants-2000_07
ORD IDord-e9d42e6fb87d4beaadee9b7bc5f3189d
Source noteuspto-grants-2000_07