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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924440Generated: November 1, 2026

Morpholine → Ethyl 3-{[(benzyloxy)carbonyl]amino}-7-morpholin-4-ylquinoline-2-carboxylate

https://huagongshe.com/reaction/924440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
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—
ProductEthyl 3-{[(benzyloxy)carbonyl]amino}-7-morpholin-4-ylquinoline-2-carboxylateHCID 8672689198.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate (300 mg, 0.7 mmol), morpholine (120 mg, 1.4 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-butanol (10 mL) in a sealed vial was purged with nitrogen then heated at 100° C. for 1 h. The solution was allowed to cool then and diluted with EtOAc, and the mixture was filtered through diatomaceous earth. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by flash chromatography on 40 g of silica gel, eluting with 0-100% EtOAc in hexanes, to give the sub-title compound (0.3 g, 20%). LCMS (ESI) calc. for C24H26N3O5 [M+H]+: m/z=436.2. found: 436.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278950B2
Source datasetuspto-grants-2016_03
ORD IDord-f885fa28c73849769ef52659a9a22e9a
Source noteuspto-grants-2016_03