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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22134543 | HCID 22134543 | — |
| Reactant | 6, 7-Dimethoxy-2-quinoxaline carboxaldehyde | HCID 22573121 | — |
| Product | Cyclohexyl-(6,7-dimethoxyquinoxalin-2-ylmethyl)-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852712B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-18dc1b1303554bae98f7737b5b480d71 |
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| Source note | uspto-grants-2005_02 |
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