Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 66693427 | HCID 66693427 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66695610 | HCID 66695610 | — |
Reaction Steps
To a solution of 410 mg (1037 μmol) of N-cyclopropyl-4-{8-[(2-methylpropyl)amino]-6-(methylsulfanyl)imidazo[1,2-b]pyridazin-3-yl}benzamide, which was prepared according to example 193, in 15 mL of DMF was added and 1912 mg (3110 μmol) OXONE (potassium peroxymonosulfate) in small portions. The mixture was stirred over night, then cooled to 0° C. and poured onto 200 mL of cold water. The precipitate was collected and dried under vacuum to yield 291 mg of the title compound as a yellow solid.
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-ac2c71edcc69470b93ac58d4ccd2da8a |
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| Source note | uspto-grants-2016_02 |
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