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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23344Generated: October 28, 2026

Cyclohexylamine → Cyclohexyl-(6,7-dimethoxyquinoxalin-2-ylmethyl)-amine

https://huagongshe.com/reaction/23344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22134543HCID 22134543—
Reactant6, 7-Dimethoxy-2-quinoxaline carboxaldehydeHCID 22573121—
ProductCyclohexyl-(6,7-dimethoxyquinoxalin-2-ylmethyl)-amineHCID 22573183—

Reaction Steps

To a 0.067 M solution of 6,7-dimethoxy-2-quinoxaline carboxaldehyde in 2:1 MeOH/1,2-dichloroethane (7.5 mL, 0.5 mmol) is added cyclohexylamine (0.11 mL, 0.9 mmol). The reaction is allowed to stir at room temperature overnight, then NaBH4 (0.038 g, 1 mmol) is added and the reaction mixture is stirred overnight. The mixture is then concentrated and chromatographed (50% EtOAc/hexanes—approximately 5% MeOH in 50% EtOAc/hexanes). The oil is dissolved in EtOAc/hexanes and treated with HCl in EtOH. The resulting solution is concentrated and the solids are triturated with isopropanol to provide a white solid after drying in vacuo at 60° C. (m.p. 185-190° C., dec.). Anal. Calcd. for C17H23N3O2.HCl: C, 60.44; H, 7.16; N, 12.44; Found: C, 60.48; H, 6.88; N, 12.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852712B2
Source datasetuspto-grants-2005_02
ORD IDord-18dc1b1303554bae98f7737b5b480d71
Source noteuspto-grants-2005_02