Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethyl 6-chloro-4-(3,5-dimethylphenylamino)pyridazine-3-carboxylate | HCID 86689770 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 73777170 | HCID 73777170 | 96% |
Reaction Steps
To a solution of ethyl 6-chloro-4-(3,5-dimethylphenylamino)pyridazine-3-carboxylate (104 mg, 340 μmol) in methanol was added ammonia in methanol (4.86 mL, 34.0 mmol) and stirred at 50° C. for 16 h. The mixture was concentrated to give 6-chloro-4-(3,5-dimethylphenylamino)pyridazine-3-carboxamide (90 mg, 325 μmol, 96%) as a brown solid, which was used directly without purification. 1H NMR (400 MHz, DMSO-d) δ ppm 10.84 (s, 1H), 8.72 (s, 1H), 8.08 (s, 1H), 7.12 (s, 1H), 6.98 (s, 2H), 6.98 (s, 1H), 6.93 (s, 1H), 2.30 (s, 6H); MS (EI/CI) m/z: 276.9 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901124B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-c700e9d459d743fab7206067d5a29f3e |
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| Source note | uspto-grants-2014_12 |
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