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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803404Generated: October 26, 2026

Ethyl 2-hydroxyisobutyrate → Bindarit

https://huagongshe.com/reaction/1803404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-hydroxyisobutyrateHCID 6653—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzyl-3-(chloromethyl)-1H-indazoleHCID 53260648—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductBindaritHCID 71354—

Reaction Conditions

Temperature90 °C

Reaction Steps

Ethyl-2-hydroxyisobutyrate (18.5 g, 140 mmol, 1.2 eq.), toluene (100 mL) and DMF (20 mL) were placed in a three-necked flask fitted with a mechanical stirrer and a reflux condenser under an inert atmosphere. A dispersion of 60% NaH (5.6 g, 140 mmol, 1.2 eq.) was added to the mixture in portions over a period of approximately 1.5 hours. A solution of 1-benzyl-3-chloromethyl-1H-indazole (30 g, 117 mmol, 1 eq.) in toluene (90 mL) and DMF (60 mL) was then added dropwise. The reaction mixture was heated to approximately 90° C. and kept at that temperature until the reaction was complete (checked by TLC, approximately 10 hours). After cooling to room temperature the mixture was washed with acidified water and water. The organic phase was concentrated under reduced pressure and the oily residue obtained was treated with 10 M NaOH (36 mL) at reflux temperature for at least 3 hours. The product, which was precipitated out by the addition of concentrated HCl, was filtered and dried. Yield: 32.3 g of white solid (85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350052B2
Source datasetuspto-grants-2013_01
ORD IDord-8051e514f88845b08a3bf09e8656c363
Source noteuspto-grants-2013_01