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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038787Generated: October 31, 2026

1,1'-Carbonyldiimidazole → Tert-butyl (1-(3-methyl-1,2,4-oxadiazol-5-yl)cyclopropyl)carbamate

https://huagongshe.com/reaction/2038787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-((tert-Butoxycarbonyl)amino)cyclopropanecarboxylic acidHCID 688396—
ReactantHCID 178465666HCID 178465666—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductTert-butyl (1-(3-methyl-1,2,4-oxadiazol-5-yl)cyclopropyl)carbamateHCID 5696565587.8%

Reaction Steps

To a solution of N-boc-amino-cyclopropanecarboxylic acid (1.01 g, 5.00 mmol) in 2 mL of DMF was added carbonyldiimidazole (0.812 g, 5.01 mmol). This reaction mixture was stirred at room temperature for 6 h. N-Hydroxy-acetamidine (0.374 g, 5.05 mmol) was added. This reaction mixture was stirred at room temperature for 2 h then heated at 100° C. for 16 h. After cooling to room temperature, the reaction mixture was diluted with water. The resultant precipitate was collected by filtration, washed with acetonitrile and water and air-dried to give 1.05 g of [1-(3-methyl-1,2,4-oxadiazol-5-yl)-cyclopropyl]-carbamic acid tert-butyl ester as a white solid, m/z 240 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575360B2
Source datasetuspto-grants-2013_11
ORD IDord-77c122b19b664064b52851fe959c7ba1
Source noteuspto-grants-2013_11