Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | HCID 89545228 | HCID 89545228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 89545209 | HCID 89545209 | — |
Reaction Steps
To (S)-tert-butyl 3-((5-fluoro-6′-methoxy-2′-(methylsulfonyl)-[2,5′-bipyrimidin]-4′-yl)amino)piperidine-1-carboxylate (0.05 g, 0.104 mmol) in MeCN (3.5 mL) was added morpholine (0.027 ml, 0.311 mmol) in a pressure tube. The reaction was heated to 100° C. for 18 h. Upon completion of the reaction, the solvent was removed and reaction was purified via column chromatography (0-50% EtOAc/Hex) to afford the desired product as a white solid. MS (m/z)=490 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221809B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-59d63289ce324ce78e4722cfba671f19 |
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| Source note | uspto-grants-2015_12 |
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