Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | TMS-Imidazole | HCID 14420972 | — |
| Reactant | HCID 20748290 | HCID 20748290 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10183130 | HCID 10183130 | 98.1% |
Reaction Steps
To a solution of N-[1′-(6-cyano-1,2,3,4-tetrahydro-2(R)-naphthalenyl)-3,4-dihydro-4(R)-hydroxyspiro[2H-1-benzopyran-2,4′-piperidin]-6-yl]amine (50 mg, 0.128 mmole) in acetonitrile under argon was added trimethylsilylimidazole (0.36 gm, 2.5 mmole) and the reaction warmed to 60 C. for 1.5 hrs. The reaction was concentrated in vacuo and purified by flash chromatography using 95/5/0.1 dichloromethane/methanol/triethylamine to give N-[1′-(6-cyano-1,2,3,4-tetrahydro-2(R)-naphthalenyl)-3,4-dihydro-4(R)-trimethylsilyloxyspiro[2H-1-benzopyran-2,4′-piperidin]-6-yl]amine as a foam (58 mg, 98%). MS m/z 462 (M+), 1H NMR (CDCL3) δ 0.09 (9 H, s), 1.4-2.1 (8 H, m), 2.4-2.9 (9 H, m), 3.2 (2 H, br, s), 4.65 (1 H, t), 6.41(1 H, dd, J=9.2 and 3.3 Hz), 6.49 (1 H, d, J=3.3 Hz), 6.52 (1 H, d, J=9.2 Hz), 7.03 (1 H, d, J=9.2 Hz), 7.22 (2 H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06838291B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-620c17afa0d04879a76ecef7d7c1de33 |
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| Source note | uspto-grants-2005_01 |
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