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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456053Generated: October 25, 2026

Dimethylformamide → 1-Methyl-1H-indazole-5-carboxaldehyde

https://huagongshe.com/reaction/456053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant5-Bromo-1-methyl-1H-indazoleHCID 22558725—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418443HCID 178418443—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-1H-indazole-5-carboxaldehydeHCID 3781859480.2%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A suspension of n-BuLi (7.33 mL, 11.73 mmol) and ethylmagnesium bromide (5.76 mL, 5.76 mmol) in 30 mL toluene was stirred at −30° C. for 30 min, then 5-bromo-1-methyl-1H-indazole (2.25 g, 10.66 mmol) in 5 mL THF was added. After stirring at −10° C. for 1 hour, anhydrous DMF (4.95 mL, 64.0 mmol) was added at −10° C. The reaction was allowed to warm to room temperature and stirred for 2 hours. The reaction was quenched with 1N HCl and concentrated in vacuo. The residue was diluted with water, extracted with DCM twice. The organic layers were combined, dried over Na2SO4 and concentrated. The crude product was purified by flash chromatography (hexane:EtOAc=10:1) to give the title compound as a white solid (1.37 g, 76%). 1H-NMR (400 MHz, DMSO-d6) δ ppm 10.02 (s, 1H), 8.41 (d, 1H), 8.31 (d, 1H), 7.86 (dd, 1H), 7.78 (d, 1H), 4.09 (s, 3H). LCMS (method A): [MH]+=161, tR=4.00 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497368B2
Source datasetuspto-grants-2013_07
ORD IDord-0784e2a63be9412981142960a5a6b351
Source noteuspto-grants-2013_07