Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (4R)-4-(hydroxyMethyl)-2-Pyrrolidinone | HCID 51669743 | — |
| Reactant | HCID 58072085 | HCID 58072085 | — |
| Product | HCID 53341128 | HCID 53341128 | — |
Reaction Steps
50.7 mg (R)-4-Hydroxymethyl-pyrrolidine-2-one (2.2) was placed in 1.5 mL of dimethylacetamaide at ambient temperature under nitrogen before 20.5 mg sodium hydride (60% dispersion in oil) was added. The reaction was stirred for 10 min and then 150 mg 5-chloro-7-[4-(tetrahydro-pyran-4-yloxy)-3-trifluoromethyl-phenyl]-[1,6]naphthyridine (6.23) was introduced and the reaction was heated to 70° C. and stirred overnight. After this time the mixture was cooled to ambient temperature and partitioned between ethyl acetate, water and some saturared sodium chloride solution. The organic layer was separated, dried over sodium sulfate, filtered and the solvent was removed from the filtrate under reduced pressure. Purification by chromatography on silica provided the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969568B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-150ab42ad4844ccc89ce142c9962256f |
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| Source note | uspto-grants-2015_03 |
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