Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Chloro-2-methylbenzenesulfonyl chloride | HCID 522734 | — |
| Reactant | 6-Quinoxalinamine,2-methyl-(9CI) | HCID 12666714 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11187117 | HCID 11187117 | 92.6% |
Reaction Steps
To a solution of 3-chloro-2-methylbenzenesulphonyl chloride (119 mg, 0.528 mmol) in dichloromethane (3 mL) was added pyridine (100 μL, 1.26 mmol) and the mixture was stirred under N2 for 5 min, after which time 6-amino-2-methylquinoxaline (80 mg, 0.50 mmol) was added. The resulting mixture was stirred for 5 h. at room temperature, then saturated NaHCO3 solution (8 mL) was added and the mixture was extracted into ethyl acetate (15 mL). The organic phase was washed with brine, dried (Na2SO4), filtered and evaporated to give a residue that was purified using flash chromatography to afford a pale pink solid (161 mg, 92%), single spot at Rf 0.67 (ethyl acetate). mp 158.7-159.3° C., HPLC purity 99+% (tR 2.23 min in 10% water-acetonitrile). 1H NMR (CDCl3): δ 8.66 (1H, s), 8.02 (1H, d, J=7.7 Hz), 7.89 (1H, d, J=8.9 Hz), 7.61 (1H, d, J=2.5 Hz), 7.55 (1H, d, J=8.2 Hz), 7.46 (11H, dd, J=8.9, 2.5 Hz), 7.23 (1H, t, J=7.9 Hz), 7.08 (1H, s, N—H), 2.76 (3H, s), 2.71 (3H, s). LCMS: 346.11 (M−). FAB-MS (MH+, C16H14ClN3O2S): calcd 348.0573, found 348.0589.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07230020B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-d5f6920034024be3ac5c32dae89dcb40 |
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| Source note | uspto-grants-2007_06 |
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