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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706669Generated: October 30, 2026

Methyl 3-(bromomethyl)benzoate → Methyl 3-((3-iodo-4-nitro-1H-indazol-1-yl)methyl)benzoate

https://huagongshe.com/reaction/706669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-(bromomethyl)benzoateHCID 517981—
Reactant2-tert-Butyl-1,1,3,3-tetramethylguanidineHCID 3571581—
ReactantHCID 178526562HCID 178526562—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-((3-iodo-4-nitro-1H-indazol-1-yl)methyl)benzoateHCID 6797610168.8%

Reaction Steps

To a slurry of 3-iodo-4-nitro-1H-indazole (1.0 g, 3.46 mmol) and methyl 3-(bromomethyl)benzoate (1.59 g, 6.92 mmol) and CH3CN (12 mL) was added 2-tert-butyl-1,1,3,3-tetramethylguanidine (0.697 mL, 3.46 mmol) dropwise, and the mixture was allowed to stir overnight at ambient temperature. The mixture was then concentrated and diluted with saturated aqueous NH4Cl (40 mL) and EtOAc (70 mL). The organic layer was separated and the aqueous phase was extracted with EtOAc (25 mL). The combined organic extracts were washed with brine, then dried over Na2SO4, filtered and concentrated. The crude product was purified by column chromatography (50% EtOAc/hexane) to provide 1.04 g (68%) of the product as a yellow/orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174981B2
Source datasetuspto-grants-2015_11
ORD IDord-35479a7493cf4efc9c15f6107b050a48
Source noteuspto-grants-2015_11