Hydrochloric Acid → [6-(3-Aminomethyl-4-fluoro-phenyl)-2-methoxy-pyrimidin-4-yl]-[2-(4-methoxy-phenyl)-ethyl]-amine hydrochloride

HRID 2110658Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2110658
[F:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[C:15]([NH:17][CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][C:23]([O:26][CH3:27])=[CH:22][CH:21]=3)[N:14]=[C:13]([O:28][CH3:29])[N:12]=2)=[CH:7][C:3]=1[CH:4]=[N:5]O.[ClH:30]>C(O)(=O)C.CCOC(C)=O.[Zn]>[ClH:30].[NH2:5][CH2:4][C:3]1[CH:7]=[C:8]([C:11]2[N:12]=[C:13]([O:28][CH3:29])[N:14]=[C:15]([NH:17][CH2:18][CH2:19][C:20]3[CH:21]=[CH:22][C:23]([O:26][CH3:27])=[CH:24][CH:25]=3)[CH:16]=2)[CH:9]=[CH:10][C:2]=1[F:1]

Komponenten

6

Versuchsvorschrift

A mixture of 2-fluoro-5-{2-methoxy-6-[2-(4-methoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzaldehyde oxime [860 mg, Example 26(a)] in acetic acid (10 mL) is treated with zinc powder (0.6 g, 9.2 mmol). After 1 hour at 20° C., the reaction mixture is filtered through Celite, concentrated, diluted with 1 M sodium hydroxide solution, and extracted with ethyl acetate. The extracts are dried over magnesium sulfate, filtered, and subjected to chromatography on silica gel eluting with 10% MeOH in DCM to provide the free base, which is treated with saturated HCl in EtOAc afford [6-(3-aminomethyl-4-fluoro-phenyl)-2-methoxy-pyrimidin-4-yl]-[2-(4-methoxy-phenyl)-ethyl]-amine hydrochloride [720 mg, Example 27]. LCMS: RT=1.88 minutes, MS: 383 (M+H). IC50=41 nM

Aufarbeitung

  1. filtrationthe reaction mixture is filtered through Celite
  2. concentrationconcentrated
  3. additiondiluted with 1 M sodium hydroxide solution
  4. extractionextracted with ethyl acetate
  5. dry with materialThe extracts are dried over magnesium sulfate
  6. filtrationfiltered
  7. customto provide the free base, which

Quellen und Nachweise

ORD-Eintrag
ord-7fdbc424f55548c2ab1177f36f6f4746
Quelldatensatz
uspto-grants-2009_04
Patentnummer
US07517889B2

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