Hydrochloric Acid → 1-[(3-ethyl-1,2,4-oxadiazol-5-yl)methyl]-6-(4-fluorophenyl)-3-(piperidin-4-yl)thieno[3,2-d]pyrimidine-2,4(1H,3H)-dione hydrochloride

HRID 1476648Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1476648
[CH2:1]([C:3]1[N:7]=[C:6]([CH2:8][N:9]2[C:14]3[CH:15]=[C:16]([C:18]4[CH:23]=[CH:22][C:21]([F:24])=[CH:20][CH:19]=4)[S:17][C:13]=3[C:12](=[O:25])[N:11]([CH:26]3[CH2:31][CH2:30][N:29](C(OC(C)(C)C)=O)[CH2:28][CH2:27]3)[C:10]2=[O:39])[O:5][N:4]=1)[CH3:2].[ClH:40]>O1CCOCC1>[ClH:40].[CH2:1]([C:3]1[N:7]=[C:6]([CH2:8][N:9]2[C:14]3[CH:15]=[C:16]([C:18]4[CH:19]=[CH:20][C:21]([F:24])=[CH:22][CH:23]=4)[S:17][C:13]=3[C:12](=[O:25])[N:11]([CH:26]3[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]3)[C:10]2=[O:39])[O:5][N:4]=1)[CH3:2]

Komponenten

4

Versuchsvorschrift

To a solution of tert-butyl 4-{1-[(3-ethyl-1,2,4-oxadiazol-5-yl)methyl]-6-(4-fluorophenyl)-2,4-dioxo-1,4-dihydrothieno[3,2-d]pyrimidin-3(2H)-yl}piperidine-1-carboxylate (360 mg, compound B65) in 1,4 dioxane (13 ml) is added a solution of hydrogen chloride in 1,4-dioxane (3 ml, 4.0 M) and the reaction mixture is stirred for 48 h at RT. Subsequently the suspension is filtered to give title compound as a solid.

Aufarbeitung

  1. filtrationSubsequently the suspension is filtered

Quellen und Nachweise

ORD-Eintrag
ord-915e3f5d41b14617a0549e235489516d
Quelldatensatz
uspto-grants-2015_04
Patentnummer
US09018175B2

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