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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182220Generated: November 2, 2026

1,2-Dichloroethane → (+/-)-2,5-Dioxo-N-(quinolin-8-ylmethyl)-3',4'-dihydro-1'H-spiro[imidazolidine-4,2'-naphthalene]-6'-carboxamide

https://huagongshe.com/reaction/1182220

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(Quinolin-8-yl)methanamineHCID 15079229—
Reactant(+/-)-6'-carboxy-3',4'-dihydro-1'H-spiro[imidazolidine-4,2'-naphthalene]-2,5-dioneHCID 18440314—
SolventDimethylformamideHCID 6228—
Product(+/-)-2,5-Dioxo-N-(quinolin-8-ylmethyl)-3',4'-dihydro-1'H-spiro[imidazolidine-4,2'-naphthalene]-6'-carboxamideHCID 9843928—

Reaction Steps

A mixture of 8-(aminomethyl)quinoline (14 mg, 0.088 mmol), (±)-6′-carboxy-3′,4′-dihydro-1′H-spiro[imidazolidine-4,2′-naphthalene]-2,5-dione (described in Intermediate 1) (15 mg, 0.058 mmol), EDC (22 mg, 0.115 mmol), and HOBT (13 mg, 0.088 mmol) was stirred in DMF (0.8 mL) at ambient temperature for 18 h. The crude mixture was purified directly by HPLC using a reversed phase C18 column and eluting with a gradient of H2O:CH3CN:CF3CO2H—90:10:0.1 to 5:95:0.1. Lyophilization provided the title compound as a tan solid. MS: m/z=401 (M+1). HRMS: m/z=401.1584; calculated m/z=401.1608 for C23H21N4O3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288559B2
Source datasetuspto-grants-2007_10
ORD IDord-c3ddfab5def74c78bed521de474c432f
Source noteuspto-grants-2007_10