Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 131730679 | HCID 131730679 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 49835672 | HCID 49835672 | — |
Reaction Steps
To a cooled with an ice-bath suspension of 5-[1-(1,3-dimethyl-1H-pyrazol-4-yl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl]-2-methoxy-nicotinic acid TFA salt (Example 124, 60 mg, 0.089 mmol) in dichloromethane (1.5 ml) containing DMF (0.005 ml) was added oxallyl chloride (0.038 ml, 0.449 mmol). The reaction mixture was stirred for 1 h at rt then cooled with an ice-bath and quenched with 8 M methylamine in ethanol (2.5 ml, 20 mmol). After 5 min stirring, the reaction mixture was evaporated to dryness and the residue purified by Prep.HPLC (H2O (0.1% TFA)/CH3CN 95:5 to 65:35). The fractions containing products were collected together, basified with NaHCO3, concentrated and the formed precipitate was filtered, washed with water and dried to give the title compound as white solid. (HPLC: tR 2.45 min (Method A); M+H=458 MS-ES; 1H-NMR (d6-DMSO, 400 MHz) 8.97 (s, 1H), 8.52-8.46 (m, 1H), 8.35-8.27 (m, 1H), 8.19-8.07 (m, 3H), 7.99-7.93 (m, 1H), 7.56-7.51 (m, 1H), 4.00 (s, 3H), 3.95 (s, 3H), 3.57 (s, 3H), 2.83 (d, 3H), 1.94 (s, 3H))
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476294B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-9c82732fb6814fb18d53a17770b75546 |
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| Source note | uspto-grants-2013_07 |
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