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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174927Generated: November 1, 2026

Ethyl Acetate → Tert-butyl 3-[(5-bromo-4-methyl-2H-indazol-2-yl)methyl]-azetidin-1-carboxylate

https://huagongshe.com/reaction/2174927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant5-Bromo-4-methyl-1H-indazoleHCID 44119232—
ReactantTert-butyl 3-(tosyloxymethyl)azetidine-1-carboxylateHCID 56777214—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 3-[(5-bromo-4-methyl-2H-indazol-2-yl)methyl]-azetidin-1-carboxylateHCID 117690535—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 21.1 g of 5-bromo-4-methyl-1H-indazole and 37.6 g of tert-butyl-3-[(tosyloxy)-methyl]azetidin-1-carboxylate in 100 ml dioxan were added 150 ml of a 1M solution of sodium bis(trimethylsilyl)amide in tetrahydrofuran at 25° C. and this was stirred for 6 hrs at 90° C. After cooling, the reaction mixture was treated with ethyl acetate and water, the organic phases separated and the aqueous phase extracted twice with 100 ml portions of ethyl acetate. The combined organic phases were washed with saturated sodium chloride solution, dried over sodium sulphate, and concentrated in vacuo after filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062041B2
Source datasetuspto-grants-2015_06
ORD IDord-20781fbff8cc45bc8a8d2d772b8723e5
Source noteuspto-grants-2015_06