Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,6-Dibromopyridazine | HCID 248852 | — |
| Reactant | 1-(Dimethylamino)-2-methylpropan-2-ol | HCID 9793738 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86662320 | HCID 86662320 | 65.1% |
Reaction Steps
In a 100 mL round bottom flask was added 1-(dimethylamino)-2-methylpropan-2-ol (1.48 g, 12.6 mmol, Eq: 1.5), THF and 3,6-dibromopyridazine (2 g, 8.41 mmol, Eq: 1.00). The flask was cooled to 0° C. followed by addition of NaH (572 mg, 14.3 mmol, Eq: 1.7) in one portion. The turbid reaction mixture was allowed to warm to room temperature and was stirred at room temperature overnight. The resultant black reaction mixture was absorbed onto silica gel and purified by LC chromatography eluting with 0-5% MeOH in 1/1 EtOAc/Hex to afford 1.5 g (65%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481540B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-40e996f4ac5b45199b6b38b6571d5db8 |
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| Source note | uspto-grants-2013_07 |
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