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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110939Generated: October 26, 2026

Water → Tert-butyl[2-(3-cyclopropyl-[1,2,4]oxadiazol-5-yl)-ethyl]-carbamate

https://huagongshe.com/reaction/2110939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-{[(tert-butoxy)carbonyl]amino}propanoateHCID 15933116—
ReactantHCID 178513214HCID 178513214—
SolventDimethylformamideHCID 6228—
ProductTert-butyl[2-(3-cyclopropyl-[1,2,4]oxadiazol-5-yl)-ethyl]-carbamateHCID 57637077—

Reaction Conditions

Temperature50 °C

Reaction Steps

3.10 g (30.96 mmol) N-hydroxy-cyclopropanecarboxamidine are placed in 10 ml dimethylformamide and molecular sieve. 1.32 g (34.06 mmol) sodium hydride (60% in mineral oil) are added. The mixture is stirred for 0.1 hours at 50° C., then 7.40 g (34.06 mmol) ethyl 3-tert-butoxycarbonylamino-propionate in 20 ml dimethylformamide are added. The reaction mixture is stirred for 3 hours at 50° C. After cooling 15 ml of water are added, the mixture is suction filtered through Celite. The 2 phases of the filtrate are separated, the aqueous phase is extracted with ethyl acetate, the combined organic phase is evaporated down. The residue is purified by chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517995B2
Source datasetuspto-grants-2009_04
ORD IDord-9f3f3e6ad548429590d893ba0dac2779
Source noteuspto-grants-2009_04