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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025542Generated: October 31, 2026

1-Hydroxybenzotriazole → 8-Hydroxy-N-methyl-N-(4-(2-phenylpropan-2-yl)benzyl)quinoline-2-carboxamide

https://huagongshe.com/reaction/1025542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant8-Hydroxyquinoline-7-carboxylic AcidHCID 231363—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-[4-(1-Methyl-1-phenylethyl)benzyl]-methylamineHCID 18333891—
SolventDichloromethaneHCID 6344—
Product8-Hydroxy-N-methyl-N-(4-(2-phenylpropan-2-yl)benzyl)quinoline-2-carboxamideHCID 6729313847.6%

Reaction Steps

TEA (42 mg, 0.42 mmol), EDC.HCl (80 mg, 0.42 mmol), HOBt (57 mg, 0.418 mmol) and N-methyl-1-(4-(2-phenylpropan-2-yl)phenyl)methanamine (50 mg, 0.21 mmol) of Preparation 1 were sequentially added to a suspension of 8-hydroxyquinoline-7-carboxylic acid (48 mg, 0.25 mmol) in DCM (2.5 mL). The resulting reaction mixture was stirred at RT overnight. The mixture was quenched with H2O and then extracted three times with DCM. The separated organics were dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, DCM:MeOH 95:5) affording the title compound (39 mg, 0.1 mmol) as a grey solid. LC-MS m/z (ESI+): 411.2 (MH+), Rt=2.42 min (Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729098B2
Source datasetuspto-grants-2014_05
ORD IDord-2f4323f60f0343f0b75e2947b552144f
Source noteuspto-grants-2014_05