Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007875Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 11124529, compound

https://huagongshe.com/reaction/1007875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantHCID 9822187HCID 9822187—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 11124529HCID 1112452914%

Reaction Steps

A mixture of 5-ethyl-9,10-difluoro-5-hydroxy-1,4,5,13-tetrahydro-3H,15H-oxepino[3′,4′:6,7]indolizino[1,2-b]quinoline-3,15-dione (200 mg, 0.526 mmol, example 18), N-Boc-glycine (185 mg, 1.051 mmol) and a catalytic quantity of 4-dimethylaminopyridine (20 mg) in anhydrous pyridine (10 ml) is treated at 0° C. and under argon with dicyclohexylcarbodiimide (239 mg, 1.16 mmol), then agitated at ambient temperature for 48 hours. The volatiles are driven off under vacuum and the residue is chromatographed (SiO2, 1% methanol in chloroform) in order to produce the desired intermediate (40 mg, 14%), a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797715B1
Source datasetuspto-grants-2004_09
ORD IDord-54b06bc2fbea46ceb2eb287e9b3f29d8
Source noteuspto-grants-2004_09