Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50436Generated: October 28, 2026

Tetrabutylammonium Fluoride → HCID 21875586, compound

https://huagongshe.com/reaction/50436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 67098924HCID 67098924—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21875586HCID 2187558692%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-{[tert-butyl(dimethyl)silyl]oxy}-2-ethyl-1-(4-{2-[({[(4-methylphenyl)sulfonyl]amino}carbonyl)amino]ethyl}phenyl)-1H-benzimidazole (step 5, 78 mg, 0.13 mmol) in THF (5 mL) was added tetrabutylammonium fluoride (1.0 M solution in THF, 0.16 mL, 0.16 mmol) at 0° C. The mixture was stirred at 0° C. for 2.5 h, then concentrated. The residue was dissolved in water (30 mL) and extracted with dichloromethane (50 mL). The organic layer was dried (Na2SO4) and concentrated. The residue was purified by flash column chromatography on silica gel eluting with dichloromethane/methanol (gradient elution from 20:1 to 10:1) to afford 57 mg (92%) of the title compound as white amorphous: MS (ESI) m/z 479 (M+M)+; 1H-NMR (DMSO-d6) δ 7.76 (2H, d, J=7.6 Hz), 7.35-7.39 (6H, m), 6.9 (1H, s), 6.85 (1H, d, J=8.6 Hz), 6.65 (1H, d, J=8.6 Hz), 6.51 (1H, br.s), 3.17 (2H, br.s), 2.76 (2H, t, 6.6 Hz), 2.67 (2H, q, J=7.6 Hz), 2.34 (3H, s), 1.20 (3H, t, J=7.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710054B2
Source datasetuspto-grants-2004_03
ORD IDord-720eca69918546f4a48e8ee98bd068a9
Source noteuspto-grants-2004_03