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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911436Generated: November 2, 2026

Trimethylaluminum → HCID 178489767, compound

https://huagongshe.com/reaction/1911436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylaluminumHCID 16682925—
Reactantethyl 4-((3R,5S)-3,4,5-trimethylpiperazin-1-yl)benzoateHCID 57440416—
ReactantHCID 178489815HCID 178489815—
SolventTolueneHCID 1140—
ProductHCID 178489767HCID 17848976733.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

A 2M solution of trimethylaluminium (2.500 mL, 5.00 mmol) in toluene, was added dropwise to a stirred suspension of ethyl 4-((3R,5S)-3,4,5-trimethylpiperazin-1-yl)benzoate (0.643 g, 2 mmol) and 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (0.495 g, 2.00 mmol) in toluene (10 mL) at room temperature. The solution was then heated at 60° C. for 18 h. The reaction mixture was cooled and quenched with methanol (15 ml) and 2N hydrochloric acid (5 ml). The crude reaction mixture was purified by ion exchange chromatography on a SCX column, eluting with 7N ammonia in methanol. The appropriate fractions were evaporated to give an oil. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 10% 2.5N ammonia/MeOH in DCM. Pure fractions were evaporated to dryness to afford, on crystallisation from DCM/diethyl ether, the title compound (0.322 g, 33.7%) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-ebc42faaaf3d4c048ee052bc442fb854
Source noteuspto-grants-2013_12