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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723227Generated: November 2, 2026

Methyl iodide → Methyl 4-[3-methoxy6-nitroindazol-1-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/1723227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodiumHCID 5360545—
ReactantHCID 178497911HCID 178497911—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-[3-methoxy6-nitroindazol-1-ylmethyl]-3-methoxybenzoateHCID 2336585928%

Reaction Steps

Indazole (T) (1.68 g.) was added to a solution of sodium (0.108 g.) in methanol (1.0 ml.). After stirring for 5 minutes, iodomethane (0.32 ml.) was added and stirring continued for 18 hours. The mixture was diluted with ethyl acetate, washed with water and brine, then dried (MgSO4) and evaporated. The residue was purified by flash chromatography on silica gel (130 g.), eluting with 2:98 v/v ethyl acetate:dichloromethane to give methyl 4-[3-methoxy-6-nitroindazol-1-ylmethyl]-3-methoxybenzoate (U) (0.481 g., 28%) as a yellow solid, with satisfactory NMR spectral data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859692
Source datasetuspto-grants-1989_08
ORD IDord-aa10def5dadc46c4a5b06e70febced2c
Source noteuspto-grants-1989_08