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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59802Generated: October 26, 2026

Isoamyl nitrate → Methyl 4-iodo-1H-indazole-6-carboxylate

https://huagongshe.com/reaction/59802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl nitrateHCID 10985—
ReactantHCID 67512060HCID 67512060—
SolventAcetic AcidHCID 176—
ProductMethyl 4-iodo-1H-indazole-6-carboxylateHCID 2472811991%

Reaction Steps

To a solution of 3-amino-5-iodo-4-methyl-benzoic acid methyl ester (1.22 g, 4.21 mmol) in acetic acid (20 mL) was added isoamyl nitrate (0.675 mL, 4.63 mmol). The mixture was stirred at room temperature for 30 minutes and then concentrated under reduced pressure. The residue was partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The organic layer was separated, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography to give 1.15 g (91%) of 4-iodo-1H-indazole-6-carboxylic acid methyl ester, MS (M+H)=303.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440956B2
Source datasetuspto-grants-2016_09
ORD IDord-70809c7613524ef497c67b64df382b7e
Source noteuspto-grants-2016_09