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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989275Generated: October 25, 2026

Dicyclohexylcarbodiimide → (S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/989275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxyacetamidineHCID 30926—
ReactantBoc-L-ValineHCID 83693—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product(S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazoleHCID 29550895—

Reaction Steps

A solution of BOC-L-valine (4.34 g, 20.0 mmol) in dichloromethane (20 mL) was cooled to 0° C. and treated dropwise with a solution of dicyclohexylcarbodiimide (2.06 g, 10.0 mmol) in dichloromethane (5 mL). After 1 hour the white solid which had formed was removed by filtration and the filtrate concentrated under reduced pressure. The residue was dissolved in pyridine (15 mL) and treated with acetamidoxime (488 mg, 6.6 mmol) in pyridine (5 mL) and the mixture heated at reflux for 1 hour. The pyridine was evaporated under reduced pressure and the residue partitioned between ethyl acetate and water. The organic phase was washed several times with water, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel using 10% ethyl acetate in hexanes to elute the product (0.62 g, 25%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638937B2
Source datasetuspto-grants-2003_10
ORD IDord-ec565e0f3db14af3913cb80f76cf9c43
Source noteuspto-grants-2003_10