Tetrabutylammonium Fluoride → 5-(3,5-Dicyano-2,6-dimethyl-1,4-dihydro-pyridin-4-yl)-3-(2-hydroxy-ethylamino)-indazole-1-carboxylic acid tert-butyl ester

HRID 218497Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 218497
[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([CH:17]3[C:22]([C:23]#[N:24])=[C:21]([CH3:25])[NH:20][C:19]([CH3:26])=[C:18]3[C:27]#[N:28])=[CH:14][CH:15]=2)[C:10]([NH:29][CH2:30][CH2:31][O:32][Si](C(C)(C)C)(C)C)=[N:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1>[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([CH:17]3[C:18]([C:27]#[N:28])=[C:19]([CH3:26])[NH:20][C:21]([CH3:25])=[C:22]3[C:23]#[N:24])=[CH:14][CH:15]=2)[C:10]([NH:29][CH2:30][CH2:31][OH:32])=[N:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Komponenten

4

Versuchsvorschrift

Crude 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethylamino]-5-(3,5-dicyano-2,6-dimethyl-1,4-dihydro-pyridin-4-yl)-indazole-1-carboxylic acid tert-butyl ester (6.58 g), from Synthetic Example 21, was dissolved in THF (350 mL), under Argon, and a solution of TBAF in THF (1M, 28.5 mL) was added. The mixture was stirred overnight at room temperature. The mixture was quenched with saturated ammonium chloride solution, diluted with water and extracted with EtOAc. The combined organic extracts were washed with brine, dried and concentrated to give crude 5-(3,5-dicyano-2,6-dimethyl-1,4-dihydro-pyridin-4-yl)-3-(2-hydroxy-ethylamino)-indazole-1-carboxylic acid tert-butyl ester which was used in the next step without further purification.

Aufarbeitung

  1. customThe mixture was quenched with saturated ammonium chloride solution
  2. additiondiluted with water
  3. extractionextracted with EtOAc
  4. washThe combined organic extracts were washed with brine
  5. customdried
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-0f562f5cda834d10b836f541fd39e708
Quelldatensatz
uspto-grants-2012_06
Patentnummer
US08198456B2

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