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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960137Generated: October 30, 2026

Hexamethyldisilazane → {3-[(5-biphenyl-4-yl-6-fluoro-1H-benzimidazol-2-yl)oxy]phenyl}phosphonic acid

https://huagongshe.com/reaction/1960137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
ReactantBromotrimethylsilaneHCID 76113—
Reactant[3-(5-biphenyl-4-yl-6-fluoro-1H-benzoimidazol-2-yloxy)-phenyl]-phosphonic acid diisopropyl esterHCID 86658719—
SolventDichloromethaneHCID 6344—
Product{3-[(5-biphenyl-4-yl-6-fluoro-1H-benzimidazol-2-yl)oxy]phenyl}phosphonic acidHCID 58482531—

Reaction Steps

To a solution of compound 13-8 (40 mg, 0.073 mmol) in 3 mL of CH2Cl2 was added hexamethyldisilizane (0.3 mL), followed by bromo trimethylsilane (0.1 mL, 0.74 mmol). The reaction was allowed to stir for 18 h at ambient temperature. The organic solvent was removed in vacuo, followed by the addition of H2O (1 mL). The crude product was sonicated and yielded a white suspension. Solvent was removed in vacuo and the product was dissolved in DMSO (1.5 mL). The product was purified by prepatory HPLC using a 30-80% CH3CN with 0.05% trifluoroacetic acid gradient over 20 minutes. The pure fractions were combined and lyophilized to give the desired title compound 13-9. 1H NMR δ 7.35-7.41 (2H, m), 7.48-7.51 (3H, m), 7.56-7.66 (6H, m), 7.72-7.77 (4H, m); LC-MS: m/e 461(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410284B2
Source datasetuspto-grants-2013_04
ORD IDord-9b9bb6e2735f4bbf969342d3fd027a62
Source noteuspto-grants-2013_04