Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 59513692 | HCID 59513692 | — |
| Product | HCID 59511429 | HCID 59511429 | 74% |
Reaction Steps
N-(3-{3-[2-({3-[(2-Chloroethyl)oxy]phenyl}amino)-4-pyrimidinyl]pyrazolo[1,5-a]pyridin-2-yl}phenyl)-2,2,2-trifluoroacetamide (0.500 g, 0.850 mmol) was dissolved in pyrrolidine and heated to 50° C. for 18 h. The reaction was cooled upon completion and absorbed directly onto silica gel. The crude product was purified via column chromatography using a 0-20% gradient of EtOAC/MeOH w/NH4OH to afford the desired product (310 mg, 74% yield) as a yellow solid. ES-LCMS m/z 492 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812022B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-6d8e2ccd5811417783101bc5234fa18e |
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| Source note | uspto-grants-2010_10 |
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