HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897836Generated: October 31, 2026
Maleic Acid → N2-{4-[4-amino-1-(2-morpholinoethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}-1-methyl-1H-2-indolecarboxamide dimaleate
https://huagongshe.com/reaction/897836
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | N2-{4-[4-amino-1-(2-morpholinoethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}-1-methyl-1H-2-indolecarboxamide | HCID 22347049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N2-{4-[4-amino-1-(2-morpholinoethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}-1-methyl-1H-2-indolecarboxamide dimaleate | HCID 86586281 | 43.3% |
Reaction Steps
To a mixture of N2-{4-[4-amino-1-(2-morpholinoethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}-1-methyl-1H-2-indolecarboxamide (0.048 g, 0.091 mmol) in warm ethyl acetate (2 mL) was added a solution of maleic acid (0.021 g, 0.18 mmol) in warm ethyl acetate (1 mL). A precipitate formed immediately. The reaction mixture was allowed to cool to ambient temperature and the precipitate was collected by filtration, washed with ethyl acetate (5 mL), and dried in vacuo to afford N2-{4-[4-amino-1-(2-morpholinoethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}-1-methyl-1H-2-indolecarboxamide dimaleate as a light brown solid (0.030 g, 0.039 mmol): 1H NMR (d6-DMSO, 400 MHz): δH 9.45 (1H, s), 8.31 (1H, s), 8.15 (1H, d, J=8.0 Hz), 7.71 (1H, d, J=8.0 Hz), 7.59 (1H, d, J=8.4 Hz), 7.31-7.35 (4H, m), 7.16 (1H, t, J=7.4 Hz), 6.17 (4H, s), 4.72-4.73 (2H, m), 4.04 (3H, s), 3.96 (3H, s), 3.72-3.79 (4H, m), and 3.10-3.30 (6H, obscured by water peak); RP-HPLC (Hypersil C18, 5 μm 100 Å, 15 cm; 5%-100% acetonitrile-0.1 M ammonium acetate over 15 min, 1 mL/min). Rt 11.08 min. MS: M+527.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06921763B2 |
|---|
| Source dataset | uspto-grants-2005_07 |
|---|
| ORD ID | ord-cb6e580511e84d26a0ad8f3ec19bd34d |
|---|
| Source note | uspto-grants-2005_07 |
|---|