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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924485Generated: October 31, 2026

Potassium Phosphate, Tribasic → 3-{[(Benzyloxy)carbonyl]amino}-7-(4-methyl-3-oxopiperazin-1-yl)quinoline-2-carboxylic acid

https://huagongshe.com/reaction/924485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Methylpiperazin-2-oneHCID 4399042—
Reactant2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
ReactantEthyl 3-(((benzyloxy)carbonyl)amino)-7-bromoquinoline-2-carboxylateHCID 86726857—
Catalystpalladium(II) acetateHCID 167845—
Solventtert-ButanolHCID 6386—
Product3-{[(Benzyloxy)carbonyl]amino}-7-(4-methyl-3-oxopiperazin-1-yl)quinoline-2-carboxylic acidHCID 867269309.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate (250 mg, 0.58 mmol), 1-methylpiperazin-2-one (130 mg, 1.2 mmol), Pd(OAc)2 (20 mg), dicyclohexyl(2′,6′-diisopropoxybiphenyl-2-yl)phosphine (41 mg, 0.087 mmol), and K3PO4 (490 mg, 2.3 mmol) in tert-butyl alcohol (8 mL) was purged with nitrogen then heated at 100° C. in a sealed vial for 3 h. The mixture was then allowed to cool and EtOAc and water were added. The resulting layers were separated and organic layer was concentrated under reduced pressure. To the resulting bright-yellow solid, 2 mL of dioxane, 2 mL of 2 M NaOH were added. The mixture was heated in 80° C. oil bath with stirring for 0.5 h, then allowed to cooled and neutralized with 4 mL of with 1 M HCl. The red solid formed was collected by filtration and air-dried overnight to give the sub-title compound (24 mg, 9.5%). LCMS calc. for C26H33N8O2 [M+H]+: m/z=489.3. found: 435.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278950B2
Source datasetuspto-grants-2016_03
ORD IDord-7bfa183977c545eda4a7f7e17ae8994f
Source noteuspto-grants-2016_03