Tetrabutylammonium Fluoride → methyl ((3S,4S)-1-(2-chloro-5-cyano-3-((7-cyano-4-(ethylamino)imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)-3-hydroxypiperidin-4-yl)carbamate

HRID 1430880Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1430880
[Si]([O:8][C@H:9]1[C@H:14]([NH:15][C:16](=[O:19])[O:17][CH3:18])[CH2:13][CH2:12][N:11]([C:20]2[CH:25]=[C:24]([C:26]#[N:27])[CH:23]=[C:22]([NH:28][C:29]3[N:34]=[C:33]([N:35](CC)[CH2:36][C:37]4C=CC(OC)=CC=4)[C:32]4=[N:47][CH:48]=[C:49]([C:50]#[N:51])[N:31]4[N:30]=3)[C:21]=2[Cl:52])[CH2:10]1)(C(C)(C)C)(C)C.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>O1CCCC1>[Cl:52][C:21]1[C:22]([NH:28][C:29]2[N:34]=[C:33]([NH:35][CH2:36][CH3:37])[C:32]3=[N:47][CH:48]=[C:49]([C:50]#[N:51])[N:31]3[N:30]=2)=[CH:23][C:24]([C:26]#[N:27])=[CH:25][C:20]=1[N:11]1[CH2:12][CH2:13][C@H:14]([NH:15][C:16](=[O:19])[O:17][CH3:18])[C@@H:9]([OH:8])[CH2:10]1

Komponenten

4

Edukt 2

HCID 2724141Tetrabutylammonium FluorideHCID 131732392methyl ((3R,4R)-3-((tert-butyldimethylsilyl)oxy)-1-(2-chloro-5-cyano-3-((7-cyano-4-(ethyl(4-m ethoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)piperidin-4-yl)carbamate

Produkt 1

HCID 89932123methyl ((3S,4S)-1-(2-chloro-5-cyano-3-((7-cyano-4-(ethylamino)imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)-3-hydroxypiperidin-4-yl)carbamateAusbeute 133,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

methyl ((3R,4R)-3-((tert-butyldimethylsilyl)oxy)-1-(2-chloro-5-cyano-3-((7-cyano-4-(ethyl(4-m ethoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)piperidin-4-yl)carbamate (140 mg, 0.188 mmol) was dissolved into Tetrahydrofuran (2 mL). TBAF 1M in THF (0.244 mL, 0.244 mmol) was added. The mixture was stirred at r.t. overnight. The mixture was concentrated to dryness, then diluted with EtOAc (50 ml) and washed with sat. NaHCO3. The water layer was extracted with 20 ml EtOAc. The combined organic layer was washed with brine, dried over MgSO4, filtered and concentrated to dryness to give 128 mg of product, which was used further without purification.

Aufarbeitung

  1. concentrationThe mixture was concentrated to dryness
  2. additiondiluted with EtOAc (50 ml)
  3. washwashed with sat. NaHCO3
  4. extractionThe water layer was extracted with 20 ml EtOAc
  5. washThe combined organic layer was washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-81f8376b5772470b8f930a52910d1725
Quelldatensatz
uspto-grants-2015_01
Patentnummer
US08940736B2

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