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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546089Generated: October 26, 2026

Methanol → 3-(3-Amino-pyrazol-1-ylmethyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/546089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHydrazineHCID 9321—
ReactantHCID 67191930HCID 67191930—
CatalystNickelHCID 935—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-(3-Amino-pyrazol-1-ylmethyl)-benzoic acid methyl esterHCID 6718991569.1%

Reaction Steps

The 3-(3-nitro-pyrazol-1-ylmethyl)-benzoic acid methyl ester (1.78 g, 6.82 mmol) was dissolved in ethyl acetate (5 mL) and methanol (5 mL) was added. While stirring, a 50% slurry of raney nickel in water (1 mL) was added followed by hydrazine (1.5 mL). Immediate effervescence was observed. The reaction continued to stir and bubble for 30 min. The reaction was passed through a plug of celite and concentrated in vacuo to give a yellow oil. The oil was taken up in ethyl acetate (100 mL), washed with water (2×20 mL), saturated aqueous brine solution (20 mL), dried over magnesium sulfate and concentrated in vacuo. Purification by ISCO flash column chromatography (Teledyne Isco RediSep Flash Column 120 g; 15% ethyl acetate/hexanes to 100% ethyl acetate/hexanes) afforded 3-(3-amino-pyrazol-1-ylmethyl)-benzoic acid methyl ester (1.09 g, 69%) as a beige solid: H1-NMR (400 MHz, DMSO-d6) δ 3.83 (3H, s), 4.57 (2H, bs), 5.09 (2H, s), 5.41 (1H, d, J=2.0 Hz), 7.44-7.46 (3H, m), 7.76 (1H, bs), 7.82-7.84 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935699B2
Source datasetuspto-grants-2011_05
ORD IDord-eecad71be342413e8c30bafea1b1c79c
Source noteuspto-grants-2011_05