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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186246Generated: October 30, 2026

Trimethylaluminum → HCID 53846720, compound

https://huagongshe.com/reaction/2186246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 54185929HCID 54185929—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 53846720HCID 53846720176%

Reaction Steps

To a solution of of (2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)amine (1.44 g, 4.73 mmol) in 40 mL of methylene chloride at ambient temperature was added trimethylaluminum (14.2 mL of a 2.0 M solution in toluene, 28.4 mmol) dropwise. The resulting solution was allowed to stir until no more gas evolution was observed (˜15 min). To this solution was added 1-[(4-methoxy)phenyl]-3-(hydroxymethyl)-5-(methoxycarbonyl)pyrazole (1.24 g, 4.73 mmol) in 10 mL of methylene chloride. The resulting solution was stirred at 40° C. for 16 h and then was cooled to ambient temperature and quenched by the addition of saturated aq NH4Cl. After diluting with ethyl acetate, the organic layer was washed with 10% aq HCl, saturated aq NaHCO3 and brine, dried (MgSO4), filtered through a pad of silica gel and concentrated in vacuo. The solid residue was recrystallized from hexanes/ethyl acetate to afford 1.7 g (68%) of the title compound. LRMS (ES+): 557.1 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403620B1
Source datasetuspto-grants-2002_06
ORD IDord-0a803033044d4cd691adefb5c5ac9c14
Source noteuspto-grants-2002_06