Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 23153704 | HCID 23153704 | — |
| Reactant | Monomethylamine methanol | HCID 57454252 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 135599845 | HCID 135599845 | — |
Reaction Steps
Methylamine/methanol solution (3 ml) was added to a methanol solution of 307 mg (0.97 mmol) of ethyl 6-(4-methoxyphenyl)[1,2,4]triazolo[4,3-b]pyridazine-3-carboxylate, and stirred at room temperature for 14 hours. The reaction liquid was concentrated under reduced pressure, and 2 ml (2.00 mol) of a dichloromethane solution of 1 M boron tribromide was added to a chloroform solution (4 ml) of the resulting residue, and stirred overnight at room temperature. Water was added to the reaction liquid, extracted with chloroform, and the organic layer was washed with saturated saline water. This was dried with anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 65 mg of a crude product of 6-(4-hydroxyphenyl)-N-methyl[1,2,4]triazolo[4,3-b]pyridazine-3-carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07645756B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-349aee284b504ac7bfd270b430c5123d |
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| Source note | uspto-grants-2010_01 |
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