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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913948Generated: November 2, 2026

Acetonitrile → HCID 57545990, compound

https://huagongshe.com/reaction/913948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPerfluoro-1-butanesulfonyl fluorideHCID 67814—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantN-Ethyl-N-(propan-2-yl)propan-2-amine--hydrogen fluoride (1/3)HCID 45108321—
ReactantHCID 57545941HCID 57545941—
SolventDiethyl EtherHCID 3283—
ProductHCID 57545990HCID 5754599095.1%

Reaction Steps

To a solution of tert-butyl 4-((1-(5-chloro-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-7-yl)-2-hydroxyethoxy)methyl)-4-(4-fluorophenyl)piperidine-1-carboxylate (440 mg, 0.694 mmol) in ACETONITRILE (0.1 mL, 1.915 mmol) at room temperature was added diisopropylethylamine (0.545 mL, 3.12 mmol), Diisopropylethylamine trihydrofluoride (197 mg, 1.041 mmol), and perfluoro-1-butanesulfonyl fluoride (0.249 mL, 1.387 mmol). The reaction was stirred at room temperature overnight. It was then poured into sat'd NaHCO3 and diluted with ether. The ether layer was washed with water and brine, dried over MgSO4, filtered and concentrated. The crude product was purified by silica gel column chromatography (15%-20% EtOAc/Hex) to give title compound (420 mg, 0.660 mmol, 95% yield) as a colorless film. LC/MS (HPLC method 3): tR=4.33 min, 636.3(MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026257B2
Source datasetuspto-grants-2011_09
ORD IDord-955e444348f348848e66b46f4410944e
Source noteuspto-grants-2011_09