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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662060Generated: October 30, 2026

Dimethylformamide → Methyl 1-methyl-1H-indazole-4-carboxylate

https://huagongshe.com/reaction/1662060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 1H-indazole-4-carboxylateHCID 6623327—
SolventWaterHCID 962—
ProductMethyl 1-methyl-1H-indazole-4-carboxylateHCID 37818679—
ProductMethyl 2-methyl-2H-indazole-4-carboxylateHCID 37818684—

Reaction Steps

To a mixture of sodium hydride (522 mg) and DMF (30 ml) was added methyl 1H-indazole-4-carboxylate (2.0 g) under ice-cooling, followed by stirring for 20 minutes. To the reaction mixture was added methyl iodide (1.41 ml), followed by stirring under ice-cooling for 30 minutes, and further at room temperature for 1 hour. The reaction mixture was ice-cooled, and water (100 ml) was added thereto, followed by stirring for 15 minutes. The insolubles were removed by filtration and the filtrate was extracted with ethyl acetate (80 ml). The organic layer was washed with a saturated sodium bicarbonate solution and saturated brine in this order and dried over anhydrous magnesium sulfate. The solvent was then removed by evaporation under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1→1:1) to obtain methyl 1-methyl-1H-indazole-4-carboxylate (900 mg) as a pale yellow solid and methyl 2-methyl-2H-indazole-4-carboxylate (600 mg) as a pale red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030489B2
Source datasetuspto-grants-2011_10
ORD IDord-e18190eb4cae476dba9a9353920d7e64
Source noteuspto-grants-2011_10