HuagongsheHuagongshe Chemistry Print Report · For research reference only
Maleic Acid → HCID 131724236, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | HCID 22347030 | HCID 22347030 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131724236 | HCID 131724236 | 92.4% |
Reaction Steps
1-[1-(1-isopropyl-4-piperidinyl)-4-piperidinyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (Intermediate F) (132 mg, 0.258 mmol) was dissolved in 30 ml of hot ethyl acetate and maleic acid(90 mg, 0.774 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 205 mg of 1-[1-(1-isopropyl-4-piperidinyl)-4-piperidinyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine, trimaleate salt. 1H NMR (DMSO) 1.26 (d, J=6.34 Hz, 6H), 1.90 (m, 2H), 2.23(m,4H), 2.50 (m, 2H), 3.53 (bm, 9H), 5.08 (m, 1H), 7.16 (m, 5H), 7.44 (m, 2H), 7.67 (d, J=8.30 Hz, 2H), 8.28 (s, 1H); LC/MS (MH+32 512).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06660744B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-e591f6c3885c4ffc83892fd22dcc378e |
| Source note | uspto-grants-2003_12 |