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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897571Generated: October 25, 2026

Maleic Acid → HCID 178488218, compound

https://huagongshe.com/reaction/897571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AcidHCID 444266—
ReactantHCID 178488217HCID 178488217—
SolventEthyl AcetateHCID 8857—
ProductHCID 178488218HCID 178488218109.4%

Reaction Steps

trans-N1-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-2-methoxyphenyl)-4-(trifluoromethoxy)benzamide (520 mg, 0.832 mmol) was dissolved in hot ethyl acetate (55 mL) and maleic acid (290 mg, 2.497 mmol) in hot ethyl acetate (5 mL) was added. The reaction mixture was stirred at room temperature for 5 hours. The solid was collected by filtration to give trans-N1-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-2-methoxyphenyl)-4-(trifluoromethoxy)benzamide, dimaleate salt (780 mg, 96%). 1H NMR (DMSO-d6) δ 1.60 (m, 2H), 2.06 (m, 6H), 2.68 (s, 3H), 2.83-3.17 (bm, 9H), 3.93 (s, 3H), 4.72 (m, 1H), 6.18 (s, 6H), 7.28 (d, J=8.14 Hz, 1H), 7.33 (s, 1H), 7.54 (d, J=8.47 Hz, 2H), 8.01 (d, J=8.12 Hz, 1H), 8.10 (d, J=8.69 Hz, 2H), 8.26 (s, 1H), 9.69 (s, 1H). LCMS (Finigan-Column: Pecosphere, C18, 3 um, 33×4.6 mm. Eluents: 0% B/A to 100% B/A in 4 min. (B: acetonitrile, A: 50 mM ammonia acetate buffer, pH 4.5), 3.0 mL/min.): MH+=625.4, Rt=2.21 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-09ecc73998744cdcbeca84d620bfb3b0
Source noteuspto-grants-2005_07