Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804568Generated: October 31, 2026

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

https://huagongshe.com/reaction/1804568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-(((tert-butoxy)carbonyl)amino)propanoateHCID 11687095—
ReactantHCID 178449908HCID 178449908—
SolventDimethylformamideHCID 6228—
ProductTert-butyl[2-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-ethyl]-carbamateHCID 57637051—

Reaction Conditions

Temperature50 °C

Reaction Steps

2.20 g (21.54 mmol) N-hydroxy-isobutyramidine are placed in 10 ml dimethylformamide and molecular sieve. 0.948 g (23.69 mmol) sodium hydride (60% in mineral oil) are added. The mixture is stirred for 0.1 hours at 50° C., then 6.20 g (30.51 mmol) methyl 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 and 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 phases are evaporated down. The residue is purified by chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354418B2
Source datasetuspto-grants-2013_01
ORD IDord-91816947d6704168a1593d982a18d26f
Source noteuspto-grants-2013_01