Tributyltin Chloride → HCID 71279802, Verbindung

1-(2-(1,3-dioxan-2-yl)ethyl)-5-(difluoromethoxy)-3-iodo-1H-indazole (242 mg, 571 mmol) was dissolved in THF (3.00 mL). The colorless solution was cooled to −16° C. (NaCl/ice bath), isopropylmagnesium chloride 2M in THF (319 μL, 639 μmol) was added dropwise at −16° C. The reaction mixture was stirred at −16° C. for 20 min. Then, tributylchlorostannane (214 mg, 178 μL, 656 μmol) was added slowly. The reaction mixture was warmed to 25° C. and stirred for 1.5 h. The reaction mixture was quenched with saturated ammonium chloride solution, extracted with dichloromethane (3×30 mL), organics dried over MgSO4 and concentrated to a yellow oil. The residue was dried under high vacuum and taken into next step without further purification yielding 1-(2-(1,3-dioxan-2-yl)ethyl)-5-(difluoromethoxy)-3-(tributylstannyl)-1H-indazole, assumed quantitative and used into the next step without further purification.

1. additionwas added dropwise at −16° C
2. temperatureThe reaction mixture was warmed to 25° C.
3. stirringstirred for 1.5 h
4. customThe reaction mixture was quenched with saturated ammonium chloride solution
5. extractionextracted with dichloromethane (3×30 mL)
6. dry with materialorganics dried over MgSO4
7. concentrationconcentrated to a yellow oil
8. customThe residue was dried under high vacuum
9. customtaken into next step without further purification

ORD-Eintrag

ord-b36f467b4853439ca4b39174495d2671

Quelldatensatz

uspto-grants-2014_02

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08658646B2