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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924460Generated: October 30, 2026

1-Methylpiperazine → 3-{[(Benzyloxy)carbonyl]amino}-7-(4-methylpiperazin-1-yl)quinoline-2-carboxylic acid

https://huagongshe.com/reaction/924460

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantPotassium Phosphate, TribasicHCID 62657—
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-methylpiperazin-1-yl)quinoline-2-carboxylic acidHCID 86726904—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate (300 mg, 0.7 mmol), 1-methylpiperazine (200 mg, 2 mmol), Pd(OAc)2 (20 mg), dicyclohexyl(2′,6′-diisopropoxybiphenyl-2-yl)phosphine (49 mg, 0.10 mmol), and K3PO4 (580 mg, 2.8 mmol) in tert-butyl alcohol (10 mL) was purged with N2 prior and then heated at 100° C. in a sealed vial for 2 h. The mixture was allowed to cool, diluted with EtOAc, and then filtered through a diatomaceous earth plug. The filtrate was concentrated under reduced pressure. To the resulting residue, 10 mL of dioxane and 4 mL of 2.5 M NaOH were added.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278950B2
Source datasetuspto-grants-2016_03
ORD IDord-1689f88c606d4e27b3ed67ca12a49fb3
Source noteuspto-grants-2016_03