Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 66652495 | HCID 66652495 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86682362 | HCID 86682362 | — |
Reaction Steps
To a solution of 4-[2-(2-aminopyridin-4-yl)-4-chlorophenoxy]-5-chloro-N-(ethoxymethyl)-2-fluoro-N-(5-fluoropyrimidin-2-yl)benzenesulfonamide (Preparation 15, 67 mg, 0.12 mmol) in methanol (1 mL) was added a 2.0 M solution of hydrogen chloride in water (1 mL, 2.00 mmol). The reaction mixture was heated at 60° C. for 6 hours then concentrated in vacuo. The residue was freeze dried from acetonitrile-water to afford the title compound as a white solid (69 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145407B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-a21a78233ef140b6b1be33246dcbc1d8 |
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| Source note | uspto-grants-2015_09 |
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