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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991389Generated: October 30, 2026

Stannane, tributyl(1-ethoxyethenyl)- → HCID 59128943, compound

https://huagongshe.com/reaction/1991389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
ReactantHCID 59128919HCID 59128919—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59128943HCID 59128943—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of N-(5-bromo-4-(trifluoromethyl)thiazol-2-yl)-2-(2-tert-butylphenoxy)pyridin-3-amine (Example 323a, 1.3 g, 2.75 mmol) in dioxane (30 mL) was added tributyl(1-ethoxyvinyl)tin (1.1 mL, 3.3 mmol) was degassed and Pd(PPh3)4 (160 mg, 0.14 mmol) was added. The mixture was degassed and heated at 100° C. overnight. The mixture was concentrated on vacuum, dissolved in EtOAc and treated with saturated KF solution. The solid was removed by filtering through a pad of Celite®. The filtrate was extracted with EtOAc. The organic layers were combined, washed with bring, dried over magnesium sulfate and concentrated to give crude Example A154a (1.12 g) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645778B2
Source datasetuspto-grants-2010_01
ORD IDord-c96146b4b5fe4edfa8357713e2fa671d
Source noteuspto-grants-2010_01