Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846596Generated: October 25, 2026

Methyl iodide → Methyl 1-methyl-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/846596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 1H-indazole-3-carboxylateHCID 657476—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-methyl-1H-indazole-3-carboxylateHCID 13900574—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of indazole-3-carboxylic acid methyl ester (2.76 g, 0.0159 mole) in dry dimethylformamide (20 ml) was added dropwise to a stirred suspension of 60% sodium hydride (oil dispersion) (0.67 g, 0.0176 mole) in dimethylformamide (50 ml). After the addition was completed and the evolution of the hydrogen ceased, the mixture was heated to 80° C. and then cooled to ambient temperature. A solution of methyl iodide (4.23 g, 0.030 mole) in dimethylformamide (10 ml) was added dropwise to the stirred reaction mixture. After stirring for 15 minutes, the mixture was warmed to 50° C. for 30 minutes, and then cooled to ambient temperature. The reaction mixture was diluted to a volume of 300 ml with ice/water and extracted with two 100 ml portions of methylene chloride. The extract was dried (magnesium sulfate), and concentrated to an oil. Dimethylformamide was distilled from the mixture and the residual oil was triturated with petroleum ether to obtain a solid. The solid (1.66 g, 55%) was collected by filtration and recrystallized from isooctane to give 1.20 g; mp 78°-79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137895
Source datasetuspto-grants-1992_08
ORD IDord-2a4b0acd3eb14b7c94eb24608747791b
Source noteuspto-grants-1992_08