Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | HCID 90077540 | HCID 90077540 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 90077617 | HCID 90077617 | 94.3% |
Reaction Steps
6-chloro-4-(3-(trifluoromethyl)phenylamino)-1,5-naphthyridine-3-carboxylic acid (3.6 g, 9.8 mmol) was suspended in 50 mL sulfinyl chloride. The resulting mixture was heated under stirring to 75° C. and reacted for 4 hrs while keeping at the same temperature. The reaction was naturally cooled to room temperature, and concentrated to obtain a yellow solid. The resulting solid was dispersed in 100 mL tetrahydrofuran. To the resulting mixture was added dropwise a mixture of triethylamine (3.03 g, 30 mmol) and para-methoxybenzylamine (1.6 g, 13 mmol) at 0° C. The reaction mixture was stirred at room temperature for 4 hrs, and rotary-evaporated to remove the solvent. To the residue was added 300 mL water. The resulting mixture was filtered by suction. The filter cake was washed with ethyl acetate and petroleum ether (volume ratio 1/10, 100 mL) and dried to obtain a pale yellow solid of N-(4-methoxybenzyl)-6-chloro-4-(3-(trifluoromethyl)phenylamino)-1,5-naphthyridine-3-carboxamide (4.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365572B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-f169755b1344473cb1ceb9e62d5fe50f |
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| Source note | uspto-grants-2016_06 |
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