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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116621Generated: October 29, 2026

Methyl 3-amino-4-methylbenzoate → methyl 1H-indazole-6-carboxylate

https://huagongshe.com/reaction/2116621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-amino-4-methylbenzoateHCID 337778—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Productmethyl 1H-indazole-6-carboxylateHCID 28653573.8%

Reaction Steps

To a stirred solution of methyl 3-amino-4-methylbenzoate (4.98 g, 30 mmol) in acetic acid (50 mL) was added sodium nitrite (2.29 g, 33.0 mmol) in water (5 mL) dropwise at 0° C. After 5 min a solid precipitated. The cooling bath was removed and the reaction mixture was brought to room temperature. More acetic acid (50 mL) was added to dissolve the precipitate; this was stirred for 2 h, and a clear dark solution appeared. After 4 h, acetic acid was evaporated and the residue was added to a saturated aqueous sodium bicarbonate solution; this was extracted with ethyl acetate (3×60 mL). The combined extracts were washed with brine (10 mL), dried (MgSO4) and evaporated. The residue solidified upon standing at room temperature to give an amorphous solid (3.9 g, 73%): MS (ES) m/z 177 (M+); 1H NMR (CDCl3): 10.05 (1H, br s), 8.29 (1H, s), 8.16 (1H, s), 7.86 (1H, d, J=8.0 Hz), 7.81 (1H, d, J=8.0 Hz), 3.97 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439262B1
Source datasetuspto-grants-2008_10
ORD IDord-f1cf8495aca3479b829775131d0f56ad
Source noteuspto-grants-2008_10