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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911482Generated: October 26, 2026

Hydrochloric Acid → HCID 178485325, compound

https://huagongshe.com/reaction/1911482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 4-(4-methylpiperazin-1-yl)benzoateHCID 1472668—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 178485326HCID 178485326—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 178485325HCID 17848532532.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

A 2M solution of trimethylaluminium (0.936 mL, 1.87 mmol) in toluene, was added drop-wise to a stirred suspension of 3-(2-(5-amino-1H-pyrazol-3-yl)ethyl)-N-methylbenzamide (0.183 g, 0.75 mmol) and methyl 4-(4-methylpiperazin-1-yl)benzoate (0.176 g, 0.75 mmol) in toluene (5 mL) at room temperature. The solution was then stirred at 60° C. for 18 h. The reaction mixture was cooled, poured into methanol (5 ml) and acidified with 2N HCl (15 ml). The crude product was purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH and pure fractions were evaporated to dryness to afford an oil. The crude product was purified by preparative HPLC, using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford the title compound (0.109 g, 32.6%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-b8402f3b377a49169340d5f4da544874
Source noteuspto-grants-2013_12