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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549493Generated: October 31, 2026

HCID 86614875, compound → HCID 178458983, compound

https://huagongshe.com/reaction/549493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86614875HCID 86614875—
SolventTetrabutylammonium FluorideHCID 2724141—
ProductHCID 178458983HCID 17845898333.2%

Reaction Steps

2-(9-chloro-6-(2-hydroxy-2-methylpropyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-phenanthro[9,10-d]imidazol-2-yl)isophthalonitrile (1.94 g) from Step 3 above was dissolved in TBAF (1 M in THF, 20 mL). The mixture was heated at reflux for 5 h and then quenched with water. The aqueous layer was extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated. The crude material was purified by flash chromatography on silica (50% ethyl acetate in hexanes) to provide 2-[9-chloro-6-(2-hydroxy-2-methylpropyl)-1H-phenanthro[9,10-d]imidazol-2-yl]isophthalonitrile (500 mg) as a yellow solid. 1H NMR δ (ppm) (400 MHz, Acetone-d6): 13.13 (1H, bs), 8.87 (1H, s), 8.77 (1H, s), 8.58 (1H, m), 8.43 (1H, m), 8.35 (2H, d, J=7.9 Hz), 7.99 (1H, t, J=7.9 Hz), 7.73 (2H, dd, J=1.9, 8.6 Hz), 3.51 (1H, bs), 3.08 (2H, s), 1.26 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943649B2
Source datasetuspto-grants-2011_05
ORD IDord-0458fc06e02a43388cdf1535386c045e
Source noteuspto-grants-2011_05