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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 432248Erstellt: 26. Oktober 2026

Maleic Acid → HCID 178488216, Verbindung

https://huagongshe.com/reaction/432248

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMaleic AcidHCID 444266—
Edukt4-(Dimethylamino)benzoyl chlorideHCID 4400782—
EduktHCID 178488198HCID 178488198—
LösungsmittelPyridineHCID 1049—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 178488216HCID 17848821647,7%

Reaktionsschritte

To a solution of trans-3-(4-amino-3-methoxyphenyl)-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine (500 mg, 1.15 mmol) in pyridine (5 ml) was added 4-(dimethylamino)benzoylchloride (420 mg, 2.28 mol) dropwise. The solution was stirred overnight, the solvent evaporated and the residue partitioned between dichloromethane and 2N NaOH solution. The aqueous layer was extracted with dichloromethane (×3). The organics were dried, filtered and evaporated to leave a solid which was triturated with EtOAc/Et2O (1:4) to leave a solid which was dissolved in EtOAc and treated with maleic acid (3 eqs.) to give trans-N1-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-2-methoxyphenyl)-4-(dimethylamino)benzamide (320 mg, 30%). 1H NMR (d6-DMSO)): δ H 9.05 (1H, s), 8.25 (1H, s), 8.18 (1H, d, J=8 Hz), 7.84 (2H, d, J=9.2 Hz), 7.29 (1H, s), 7.25 (1H, d, J=8 Hz), 6.78 (2H, d, J=8.8 Hz), 6.17 (6H, s), 4.71 (1H, m), 3.95 (3H, s), 3.01 (6H, s), 2.83-3.18 (9H, m), 2.68 (3H, s), 2.08 (6H, m), 1.56 (2H, m). HPLC (5.23 mins, 100%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06660744B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-8127a1456f174096b94187f9db63db07
Quellennotizuspto-grants-2003_12