Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | HCID 66691077 | HCID 66691077 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66695584 | HCID 66695584 | 42.4% |
Reaction Steps
A mixture of 28.0 mg (53 μmol) N-cyclopropyl-4-{6-(2-methoxyphenoxy)-8-[(3,3,3-trifluoropropyl)amino]imidazo[1,2-b]pyridazin-3-yl}-2-methylbenzamide which was prepared according to example 223, 44.8 mg sodium methanethiolate and 350 μL N,N-dimethylformamide was heated under microwave irradiation for 30 minutes at 120° C. The mixture was poured into water, the pH was adjusted between 7 and 8 by addition of ammonium chloride and extracted with a mixture of dichloromethane and methanol. The combined organic phases were dried over sodium sulfate. After filtration and removal of solvent the residue was purified by chromatography to give 11.5 mg (40%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255100B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-da6a2e1f1ea2434f91af482b3e2153a5 |
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| Source note | uspto-grants-2016_02 |
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