Hydrochloric Acid → 3,3,3-trifluoro-N-(4-{[3-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidin-5-yl]amino}phenyl)propanamide

HRID 1045497

Reaktionsgleichung

Reaktionsgleichung von HRID 1045497
Cl[C:2]1[C:11]2[CH2:10][N:9]([CH2:12][C:13]3[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=3)[C:8](=[O:21])[NH:7][C:6]=2[N:5]=[CH:4][CH:3]=1.[NH2:22][C:23]1[CH:28]=[CH:27][C:26]([NH:29][C:30](=[O:36])[CH2:31][C:32]([F:35])([F:34])[F:33])=[CH:25][CH:24]=1.Cl>CN1C(=O)CCC1>[F:33][C:32]([F:34])([F:35])[CH2:31][C:30]([NH:29][C:26]1[CH:27]=[CH:28][C:23]([NH:22][C:2]2[C:11]3[CH2:10][N:9]([CH2:12][C:13]4[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=4)[C:8](=[O:21])[NH:7][C:6]=3[N:5]=[CH:4][CH:3]=2)=[CH:24][CH:25]=1)=[O:36]

Komponenten

5

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

1 (52 mg, 0.17 mmol), N-(4-aminophenyl)-3,3,3-trifluoropropanamide (44 mg, 0.17 mmol), and HCl (43 μL, 4.0M in dioxane, 0.17 mmol) were suspended in NMP (1 mL), and stirred in a microwave at 150° C. for 100 min. The crude product was purified directly via HPLC to provide 100 (39% yield). LC-MS (M+H=486, obsd.=486).

Aufarbeitung

  1. customThe crude product was purified directly via HPLC

Quellen und Nachweise

ORD-Eintrag
ord-60256fb045ff4a20a61ae4daad342a47
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08569295B2

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