Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | HCID 59362928 | HCID 59362928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59362904 | HCID 59362904 | — |
Reaction Steps
Lithium aluminumhydride (2M solution in tetrahydrofuran, 1.5 mL) was added drop-wise to a solution of 1-[4-(2-morpholin-4-yl-6,7-dihydro-5H-cyclopentapyrimidin-4-ylamino)-phenyl]-cyclobutanecarboxylic acid (0.61 g, 1.52 mmol) in anhydrous tetrahydrofuran (10 mL) at 0° C. to 5° C. After addition, the reaction mixture was warmed to a temperature in the range of 15° C. to 40° C. and stirring continued for an additional 10 hours. The reaction was quenched by addition of aqueous sodium hydroxide. The precipitated solid was filtered and washed with ethyl acetate. The combined filtrates were washed with brine, dried over Na2SO4, filtered, and concentrated to yield a white solid. The title compound was afforded following purification by column chromatography (silica gel) as a white solid (0.56 g, 80% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989463B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-da7e497459f648159e7ee855fbe300da |
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| Source note | uspto-grants-2011_08 |
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