Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959618Generated: October 26, 2026

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

https://huagongshe.com/reaction/1959618

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 toluene (30 mL) was stirred at −30° C. for 30 min, and then a solution of 5-bromo-1-methyl-1H-indazole (2.25 g, 10.66 mmol) in THF (5 mL) was added. After 1 h, anhydrous DMF (4.95 mL, 64.0 mmol) was added at −10° C. The reaction mixture was allowed to warm to rt and stirred for 2 h. The reaction was quenched with saturated aqueous NH4Cl solution 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) δppm 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 numberUS08410264B2
Source datasetuspto-grants-2013_04
ORD IDord-d48de0a53c904534b1704b0981c11952
Source noteuspto-grants-2013_04