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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574261Generated: October 29, 2026

Tributyltin azide → HCID 178454218, compound

https://huagongshe.com/reaction/574261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin azideHCID 4984872—
ReactantHCID 67144622HCID 67144622—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 178454218HCID 17845421854.4%

Reaction Steps

{(R)-2-[5-[4-(3-cyano-benzyl)-piperazin-1-yl]-3-(2-fluoro-6-trifluoromethyl-benzyl)-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester (35 mg, 0.049 mmol), and azidotributyl tin (IV) (16 μl, 0.059 mmol) were dissolved at 120° C. for 10 hrs in toluene (1 mL) with stirring. The solution was cooled to room temperature, followed by the addition of azidotributyl tin (IV) (20 μl, 0.074 mmol) thereto and stirring at 120° C. for an additional 2 hrs. The solution was cooled to room temperature, diluted in dichloromethane, and washed with an aqueous saturated ammonium chloride solution and an aqueous saturated sodium chloride solution in the order. The organic layer thus formed was separated and concentrated, and the residue was purified using silica gel chromatography (eluent: dichloromethane/methanol, 6/1) and dried in a vacuum to afford 20 mg of the compound as a colorless oil (yield 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034850B2
Source datasetuspto-grants-2015_05
ORD IDord-96daa9c3cfb54d3fa32a55d4ea3e6d01
Source noteuspto-grants-2015_05