Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 58409937 | HCID 58409937 | — |
| Product | HCID 66884299 | HCID 66884299 | — |
Reaction Steps
A solution of 4-(4-methoxyphenyl)-2-(piperidin-1-yl)-9H-fluorene-1-carbonitrile (380 mg) in THF was added sodium hydride (33 mg) and was stirred at 0-5° C. for less than five minutes. After completion, the reaction solvent was evaporated under vacuum and the crude solid obtained was quenched with ice water and subsequently neutralized by dilute HCl. The precipitate thus obtained was filtered and purified on a silica gel column using ethyl acetate-hexane as eluent. Red solid; mp 210-212° C.;. FAB MS 395 (M+); IR (KBr) 2210 (CN), 1703 cm−1 (CO); HRMS calcd. for C26H22N2O2 394.1681 found 394, 1689.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946682B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-bf8de62034b140d18854bb58c0592d81 |
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| Source note | uspto-grants-2015_02 |
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