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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269872Generated: October 31, 2026

Ethyl chloroacetate → ethyl (5-nitro-1-tetrahydro-2H-pyran-2-yl-1H-indazol-4-yl)acetate

https://huagongshe.com/reaction/1269872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroacetateHCID 7751—
Reactant5-Nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazoleHCID 15147626—
ReactantMethyl 4-amino-2,5-dimethylbenzoate hydrochlorideHCID 22933657—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Productethyl (5-nitro-1-tetrahydro-2H-pyran-2-yl-1H-indazol-4-yl)acetateHCID 8659361378%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of potassium tert-butoxide (2.02 g, 18.0 mmol) in tetrahydrofuran (20 ml) was added dropwise to a solution of the 5-nitro-1-tetrahydro-2H-pyran-2-yl-1H-indazole (1.85 g, 7.48 mmol) obtained in Example 317, (d) and ethyl chloroacetate (960 μl, 9.01 mmol) in tetrahydrofuran (10 ml) at −40° C. over a period of 15 minutes, and stirred at −40° C. for 1 hour. The reaction was terminated by pouring 1N-hydrochloric acid, and the reaction solution was extracted with ethyl acetate. The extract solution was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, and then distilled under reduced pressure to remove the solvent, whereby a crude product was obtained. The crude product was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate=4/1) to obtain ethyl(5-nitro-1-tetrahydro-2H-pyran-2-yl-1H-indazol-4-yl)acetate (1.93 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-f368dba48dd646f481792908d32d4e0e
Source noteuspto-grants-2007_04