Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354834Generated: November 1, 2026

4-Nitrobenzoyl chloride → HCID 58865679, compound

https://huagongshe.com/reaction/1354834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 58865622HCID 58865622—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 58865679HCID 5886567978.6%

Reaction Steps

2,3-bis-((3R,5S)-3,5-bis-(tert-Butoxycarbonylamino)-piperidin-1-yl)-quinoxalin-6-ylamine (246) (0.067 g, 0.087 mmol) and p-nitro-benzoylchloride (0.0167 g, 0.09 mmol) were combined and dissolved in DMF (0.45 mL). iPr2EtN (0.016 mL, 0.09 mmol) was added and the mixture was shaken at room temperature for 16 h. TLC (Rf: 0.8 compared to Rf: 0.05 for compound 246 in 1:1 hexane/EtOAc) and LC-MS indicated complete coupling at this point. The mixture was diluted with EtOAc (30 mL), washed with saturated aqueous NaHCO3 (2×10 mL) and brine (2×10 mL) via extraction, dried over MgSO4 and concentrated to give the desired product (251) as an orange solid (0.063 g, 0.068 mmol, 78.6% yield). LC-MS (ESI): (exact mass: 920.48) m/e=921.8 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223759B2
Source datasetuspto-grants-2007_05
ORD IDord-d9946f841be24b5d97c76ae1d573484c
Source noteuspto-grants-2007_05