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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 246643Erstellt: 25. Oktober 2026

Tributyltin Chloride → 6-chloro-3-(tributylstannyl)-1H-indazole

https://huagongshe.com/reaction/246643

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributyltin ChlorideHCID 15096—
EduktAmmonium ChlorideHCID 25517—
EduktHCID 178418918HCID 178418918—
EduktHCID 178477877HCID 178477877—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-chloro-3-(tributylstannyl)-1H-indazoleHCID 17844822977,3%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

To a solution of 6-chloro-3-iodo-1H-indazole (337 mg, 1.21 mmol) in dry tetrahydrofuran (20 mL) was added drop-wise isopropylmagnesium chloride (1.33 mL, 2M in THF, 2.66 mmol) at −16° C. under N2 atmosphere. After stirring for 20 minutes, tributylchlorostannane (472 mg, 1.45 mmol) was added drop-wise at −16° C., and then it was warmed to 20° C. for 2 h. Then NH4Cl solution (2 mL) was added and product extracted with dichloromethane (15 mL), organic phase was washed with water (2×20 mL) and brine (2×20 mL). The organic layer was dried over Na2SO4, filtered and concentrated to afford 6-chloro-3-(tributylstannyl)-1H-indazole (413 mg, crude) as yellow oil which was used to next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658646B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-7c2d1e5327cb4a3e848a01d9cf4525d5
Quellennotizuspto-grants-2014_02