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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945304Generated: November 1, 2026

Tetrabutylammonium Fluoride → HCID 59267834, compound

https://huagongshe.com/reaction/1945304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 68527424HCID 68527424—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59267834HCID 59267834—

Reaction Conditions

Temperature80 °C

Reaction Steps

TBAF (1 M in THF) (0.9 mL, 0.9 mmol) was added to a solution of methyl 5-[(6-chloro-5-[1-(2-hydroxyethyl)-1H-indol-5-yl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazol-2-yl)oxy]-2-methylbenzoate (105 mg, 0.173 mmol) in THF (2 mL). The reaction was heated at 80° C. for 1 h. TBAF (1 M in THF) (0.2 mL, 0.2 mmol) was added and heating continuted for an additional 1 h. Volatiles were removed and the residue was dissolved in MeOH (3 mL) and treated with 2.5 N aqueous NaOH (1 mL). The mixture was stirred at 45° C. for 1.5 h, then at ambient temperature overnight. The reaction was diluted with EtOAc and the layers were separated. The organic layer was washed with 1 M aqueous HCl, water and brine, dried (Na2SO4), filtered, and concentrated. Chromatography over silica eluting with 8% MeOH/DCM containing AcOH (60 drops in 200 mL) afforded the title compound as an off-white solid. LC-MS: calculated for C25H20ClN3O4 461.90, observed m/e 462.3 (M+H)+ (Rt 1.77 min). 1H NMR (500 MHz, CD3OD): δ 7.86 (d, 1H), 7.55 (s, 1H), 7.47 (s, 1H), 7.46-7.36 (m, 3H), 7.34, (s, 1H), 7.27 (d, 1H), 7.19 (dd, 1H), 6.47 (d, 1H), 4.29 (t, 2H), 3.89 (t, 2 H), 2.61 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394969B2
Source datasetuspto-grants-2013_03
ORD IDord-1314adae322341cc97accc26bb54ac8d
Source noteuspto-grants-2013_03