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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432168Generated: November 3, 2026

Maleic Acid → HCID 178480995, compound

https://huagongshe.com/reaction/432168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AcidHCID 444266—
ReactantHCID 178480994HCID 178480994—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 178480995HCID 17848099576.4%

Reaction Steps

A solution of cis-1-[4-(4-methylpiperazino)cyclohexyl]-3-(6-phenoxy-3-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (Intermediate AJ) (0.53 g, 0.0011 mol) in a mixture of ethyl acetate (25 mL) and ethanol (4 mL) was heated at reflux and a preheated solution of maleic acid (0.51 g, 0.0044 mol) in ethyl acetate (15 mL) was added. The mixture was refluxed for another 10 min, cooled to ambient temperature and the precipitate collected by filtration, washed with ethyl acetate and dried to yield cis-1-[4-(4-methylpiperazino)cyclohexyl]-3-(6-phenoxy-3-pyridyl)-1H-pyrazolo [3,4-d]pyrimidin-4-amine dimaleate as a white solid (0.61 g, 0.00084 mol): 1H NMR (DMSO-d6, 400 MHz) 8.38 (s, 1H), 8.25 (s, 1H), 8.06 (d, 1H), 7.46 (t, 2H), 7.22 (m, 4H), 6.15 (s, 4H), 4.85 (m, 1H), 3.1 (br, 9H), 2.70 (s, 3H), 2.25 (m, 2H), 2.04 (m, 2H), 1.74 (m, 4H); RP-HPLC (Delta Pak C18, 5 μm, 300A, 15 cm; 5%-85% acetonitrile-0.1M ammonium acetate over 20 min, 1 mL/min) Rt 11.93 min. MS: MH+485.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660744B1
Source datasetuspto-grants-2003_12
ORD IDord-cc1232416ae8428bb08c191772e9ec0a
Source noteuspto-grants-2003_12