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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079323Generated: November 1, 2026

Ammonium formate → 2-(4-((S)-2-isopropylpiperazin-1-yl)-7-methylquinazolin-2-yl)phenol

https://huagongshe.com/reaction/2079323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant2-(4-((S)-4-benzyl-2-isopropylpiperazin-1-yl)-7-methylquinazolin-2-yl)phenolHCID 136121579—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(4-((S)-2-isopropylpiperazin-1-yl)-7-methylquinazolin-2-yl)phenolHCID 13612146079%

Reaction Steps

20 mg of Pd/C was added to a round-bottom flask, and the flask was flushed with nitrogen followed by evacuation of the atmosphere under vacuum. To the flask was then added a solution of 2-(4-((S)-4-benzyl-2-isopropylpiperazin-1-yl)-7-methylquinazolin-2-yl)phenol (200 mg, 0.44 mmol) in methanol, followed by the addition of ammonium formate (32 mg, 0.88 mmol). The reaction was refluxed overnight. The reaction was filtered through a bed of Celite to remove the catalyst. The solvent was evaporated to yield 2-(4-((S)-2-isopropylpiperazin-1-yl)-7-methylquinazolin-2-yl)phenol (126 mg). LC/MS: m/z 363.5 (M+H)+ at 2.13 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928107B2
Source datasetuspto-grants-2011_04
ORD IDord-b38fec3bfb6d406b8e4c07f16e068df0
Source noteuspto-grants-2011_04