Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(4-Amino-1H-pyrazol-1-yl)ethanol | HCID 28492267 | — |
| Reactant | HCID 90357141 | HCID 90357141 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | US9433622, Dmx-36 | HCID 78322872 | — |
Reaction Steps
5-(2-Chloro-pyrimidin-4-yl)-2-pyrrolidin-1-yl-nicotinonitrile (9) (31 mg, 0.108 mmol) and 2-(4-amino-pyrazol-1-yl)-ethanol (32 mg, 0.252 mmol) were dissolved in 1,4-dioxane (1 mL). 4N HCl in 1,4-dioxane (30 μL, 0.120 mmol) was added and the mixture was heated at 140° C. in the microwave (250 W, stirring) for 90 minutes. The solvent was evaporated in vacuo and the residue dissolved in DMSO (1 mL). The crude product was purified twice by reversed phase preparative LC-MS. Fractions containing desired product were combined and the solvents evaporated in vacuo. The title compound was obtained as a yellow solid (3.7 mg, 9%); LCMS, Rt=7.43 min (Method C), m/z 377 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09433622B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-b9b79ddf853e4b708f731fbf8da6add9 |
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| Source note | uspto-grants-2016_09 |
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