Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353357Generated: October 26, 2026

Sodium hydride → HCID 21101941, compound

https://huagongshe.com/reaction/1353357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 2,5-dimethylpiperazine-1-carboxylateHCID 22625934—
ReactantHCID 69514546HCID 69514546—
SolventDimethylformamideHCID 6228—
ProductHCID 21101941HCID 2110194125%

Reaction Conditions

Temperature80 °C

Reaction Steps

Sodium hydride (72 mg, 3 mmol) is added to a solution of 7-chloro-4-quinolone (359 mg, 2 mmol) in DMF. After 1 h at 40° C. N-phenyl(trifluoromethylsulfon)imide (1.0 g, 2.8 mmol) and, 1 h later, 1-tert-butoxycarbonyl-2,5-dimethylpiperazine (1.8 g, 8 mmol) is added. The reaction mixture is stirred at 80° C. for 2 days, concentrated, diluted with EtOAc, washed with water and brine, dried (Na2SO4), and concentrated. The residue is purified by reversed phase HPLC with water-MeCN-TFA to give 4-[4-(tert-butoxycarbonyl)-2,5-dimethylpiperazin-1-yl]-7-chloroquinoline (188 mg, 0.5 mmol) which is deprotected with TFA in CH2Cl2 and transformed after being washed with base into the product with 4-fluorophenyl isocyanate (31 μL, 0.27 mmol) according to method C giving the title product as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220856B2
Source datasetuspto-grants-2007_05
ORD IDord-79e5523f9ec94601abf16d5f4ceb4712
Source noteuspto-grants-2007_05