Trifluoroacetic acid → Trifluoroacetic acid

HRID 80789

Reaktionsgleichung

Reaktionsgleichung von HRID 80789
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[C:9]1[N:10]=[C:11]([N:29]2[C@H:34]([CH3:35])[CH2:33][N:32](C(OC(C)(C)C)=O)[C@@H:31]([CH3:43])[CH2:30]2)[C:12]2[CH2:18][N:17]([C:19]3[CH:24]=[C:23]([CH:25]([CH3:27])[CH3:26])[CH:22]=[CH:21][C:20]=3[CH3:28])[CH2:16][CH2:15][C:13]=2[N:14]=1.[C:44]([OH:50])([C:46]([F:49])([F:48])[F:47])=[O:45]>C(Cl)Cl>[CH3:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([CH3:1])[C:3]=1[C:9]1[N:10]=[C:11]([N:29]2[CH2:30][C@@H:31]([CH3:43])[NH:32][CH2:33][C@@H:34]2[CH3:35])[C:12]2[CH2:18][N:17]([C:19]3[CH:24]=[C:23]([CH:25]([CH3:27])[CH3:26])[CH:22]=[CH:21][C:20]=3[CH3:28])[CH2:16][CH2:15][C:13]=2[N:14]=1.[C:44]([OH:50])([C:46]([F:49])([F:48])[F:47])=[O:45]

Komponenten

5

Versuchsvorschrift

To a solution of racemic tert-butyl 4-(2-(2,6-dimethylphenyl)-6-(5-isopropyl-2-methylphenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)-(trans)-2,5-dimethylpiperazine-1-carboxylate (0.227 g, 0.389 mmol) and DCM (3 mL) at rt was added TFA (1 mL). After 25 min an additional 0.5 mL aliquot of TFA was added. After 1 h more the reaction was concentrated under reduced pressure to give 2-(2,6-dimethylphenyl)-4-((trans)-2,5-dimethylpiperazin-1-yl)-6-(5-isopropyl-2-methylphenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine as a TFA salt. MS (ESI+) m/z 484.4 (M+H)+

Aufarbeitung

  1. concentrationAfter 1 h more the reaction was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-6cce49c59faa4b3f9dc87942908d5e21
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08846656B2

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