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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766133Generated: November 2, 2026

Dicyclohexylcarbodiimide → HCID 68453063, compound

https://huagongshe.com/reaction/1766133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-tert-Butyl N-((phenylmethoxy)carbonyl)-L-glutamateHCID 107472—
ReactantOxycodoneHCID 5284603—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetoneHCID 180—
SolventAcetonitrileHCID 6342—
ProductHCID 68453063HCID 68453063—

Reaction Steps

A solution comprised of oxycodone free base, 1-1, (517 mg, 1.64 mmol), DIEA (1.5 mL, 8.6 mmol) in 9 mL of anhydrous acetonitrile was stirred at rt for 20 min and mixed with a solution containing DMAP (400 mg, 3.3 mmol), DCC (1.01 g, 4.1 mmol), and HOBt (440 mg, 3.3 mmol) in 6 mL of anhydrous acetonitrile. Cbz-L-Glu(OtBu)-OH (1.1 g, 3.3 mmol) was then added to the combined solutions. The mixture was stirred for 45 h at rt, precipitated DCU removed by filtration, and the solution concentrated under reduced pressure to give a dark-brown oil. HPLC analysis indicated that 39% of the oxycodone had been converted to 3-1. The brown oil containing crude 3-1 was dissolved in 20 mL of acetone, cooled in an ice bath for 2 h, and filtered to remove precipitated DCU. The filtrate was concentrated to dryness, and subjected to flash chromatography using a gradient of 0–10% methanol in DCM. The fractions containing 3-1 were combined and concentrated to dryness. The residue was treated with 20 mL acetone and filtered to remove precipitated DCU. The filtrate was concentrated to dryness under reduced pressure to yield partially purified 3-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230005B2
Source datasetuspto-grants-2007_06
ORD IDord-5e87b609a1dd4b3bb2da46e70be211f6
Source noteuspto-grants-2007_06