Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897425Generated: October 30, 2026

Maleic Acid → 1-[1-(1-methyl-4-piperidinyl)-4-piperidinyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine, trimaleate salt

https://huagongshe.com/reaction/897425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AcidHCID 444266—
Reactant1-[1-(1-methyl-4-piperidinyl)-4-piperidinyl](4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amineHCID 22347091—
SolventEthyl AcetateHCID 8857—
Product1-[1-(1-methyl-4-piperidinyl)-4-piperidinyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine, trimaleate saltHCID 13172423585.4%

Reaction Steps

1-[1-(1-methyl-4-piperidinyl)-4-piperidinyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (92 mg, 0.190 mmol) was dissolved in 25 ml of hot ethyl acetate and maleic acid(66 mg, 0.571 mmol) in 5 ml of hot ethyl acetate was added. After 2 hours at room temperature, the solid was filtered and then dried to give 135 mg of 1-[1-(1-methyl-4-piperidinyl)-4-piperidinyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine, trimaleate salt. 1H NMR (DMSO) 1.87(m, 2H), 2.22(m, 4), 2.45(m, 2H), 2.77(s, 3H), 2.18(bm, 9H), 5.06(m, 1H), 6.11 (s, 6H), 7.15(m, 5H), 7.45(m, 2H), 7.67(d, J=8.51 Hz, 2H), 8.27(s, 1H); LC/MS (MH+=484).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-099cdcb15c88461d80953156253a6cd6
Source noteuspto-grants-2005_07