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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759679Generated: October 31, 2026

TMS-Imidazole → HCID 10183130, compound

https://huagongshe.com/reaction/1759679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTMS-ImidazoleHCID 14420972—
ReactantHCID 20748290HCID 20748290—
SolventAcetonitrileHCID 6342—
ProductHCID 10183130HCID 1018313098.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838291B2
Source datasetuspto-grants-2005_01
ORD IDord-620c17afa0d04879a76ecef7d7c1de33
Source noteuspto-grants-2005_01