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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601624Generated: October 26, 2026

Water → [2-(3-Propyl-[1,2,4]oxadiazol-5-yl)-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/601624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-{[(tert-butoxy)carbonyl]amino}propanoateHCID 15933116—
ReactantHCID 178449909HCID 178449909—
SolventDimethylformamideHCID 6228—
Product[2-(3-Propyl-[1,2,4]oxadiazol-5-yl)-ethyl]-carbamic acid tert-butyl esterHCID 57466817—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-Hydroxy-butyramidine (0.425 g, 4.16 mmol) in DMF (2 ml) is added to a stirred suspension of sodium hydride (0.183 g of a 60% dispersion in oil, 4.58 mmol) in the presence of molecular sieves (0.4 g). The reaction flask is then immersed in a pre-heated oil bath at 50° C. and stirring continued for 5 min. 3-tert-Butoxycarbonylamino-propionic acid ethyl ester (0.904 g, 4.16 mmol) in DMF (2 ml) is added over 5 min followed by more DMF (2 ml). After 3 h at 50° C. the mixture is cooled to 0° C. and water (3 ml) is added. The mixture is allowed to warm to room temperature then filtered through Celite™ filter material, washing with ethyl acetate, and the solvent is removed. Purification by chromatography, eluting with DCM:MeOH (95:5 increasing to 85:15) affords the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902375B2
Source datasetuspto-grants-2011_03
ORD IDord-7c4b4ec3643944bea55102e646b2ee01
Source noteuspto-grants-2011_03