HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanol → 2,7-Bis-cyclohexyloxy-6-methoxy-quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-6,7-dimethoxyquinoxaline | HCID 22573137 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,7-Bis-cyclohexyloxy-6-methoxy-quinoxaline | HCID 22573179 | — |
Reaction Steps
To a DMF solution (5 mL) of NaH (0.32 g, 8 mmol) under argon, cyclohexanol (0.7 mL. 6.7 mmol) is added dropwise. The mixture is stirred at room temperature for 25 minutes, then 2-chloro-6,7-dimethoxyquinoxaline is added portionwise. The reaction is stirred for 15 minutes at room temperature, at 90° C. for 2 hours, and at 110° C. for 1 hour. The mixture is cooled, quenched with H2O, and partition between EtOAc/H2O. The organic layer is washed with H2O and brine, dried (MgSO4), and chromatographed (10% EtOAc/hexanes) to provide a waxy white solid (m.p. 75-78° C.). Anal. Calcd. for C21H28N2O3: C, 70.76; H, 7.92; N, 7.86; Found: C, 70.81; 1H, 7.79; N, 7.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852712B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-7bb381c853874411a2799197461a2745 |
| Source note | uspto-grants-2005_02 |