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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269869Generated: October 30, 2026

Acetic Anhydride → methyl 1-acetyl-6-methyl-1H-indazole-5-carboxylate

https://huagongshe.com/reaction/1269869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantIsoamyl NitriteHCID 8053—
ReactantMethyl 4-acetamido-2,5-dimethylbenzoateHCID 327521—
ReactantPotassium AcetateHCID 517044—
ReactantN-butyl-ammonium bromideHCID 21904131—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Productmethyl 1-acetyl-6-methyl-1H-indazole-5-carboxylateHCID 22933897201.8%

Reaction Steps

Acetic anhydride (0.85 ml, 9.01 mmol), n-butylammonium bromide (0.0502 g, 0.156 mmol) and potassium acetate (0.587 g, 5.98 mmol) were added to a solution of methyl 4-(acetylamino)-2,5-dimethylbenzoate (0.661 g, 2.99 mmol) in ethyl acetate (5 ml), followed by adding thereto a solution of isoamyl nitrite (0.0458 g, 3.91 mmol) in ethyl acetate (2 ml), and the resulting mixture was stirred for 8 hours with heating under reflux. Water was added thereto, followed by extraction with ethyl acetate (three times), and the extract solution was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (hexane/ethyl acetate=5/1 to 1/1). The solid thus obtained was suspended in hexane and stirred to be washed, and then it was collected by filtration and dried under reduced pressure to obtain methyl 1-acetyl-6-methyl-1H-indazole-5-carboxylate (0.0731 g, 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-220a7a2fb07e4a40839fbfb8a47d68b7
Source noteuspto-grants-2007_04