Water → Tert-butyl 4-[8-(tert-butoxycarbonylsulfamoyl)-5,8-diazaspiro[2.5]octan-5-yl]pyrrolo[2,3-d]pyrimidine-7-carboxylate

HRID 589959Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 589959
[N:1]1[C:6]2[NH:7][CH:8]=[CH:9][C:5]=2[C:4]([N:10]2[CH2:17][C:14]3([CH2:16][CH2:15]3)[N:13]([S:18]([NH2:21])(=[O:20])=[O:19])[CH2:12][CH2:11]2)=[N:3][CH:2]=1.[C:22]([O-:25])([O-:24])=O.[Cs+].[Cs+].[O:28](C(OC(C)(C)C)=O)[C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=O.O>CN(C=O)C>[C:5]([O:24][C:22]([NH:21][S:18]([N:13]1[C:14]2([CH2:16][CH2:15]2)[CH2:17][N:10]([C:4]2[C:5]3[CH:9]=[CH:8][N:7]([C:29]([O:31][C:32]([CH3:35])([CH3:33])[CH3:34])=[O:28])[C:6]=3[N:1]=[CH:2][N:3]=2)[CH2:11][CH2:12]1)(=[O:20])=[O:19])=[O:25])([CH3:9])([CH3:6])[CH3:4]

Komponenten

6

Versuchsvorschrift

7-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)-4,7-diaza-spiro[2.5]octane-4-sulfonic acid amide (intermediate 1) (1.95 mmol) was dissolved in dry DMF (15 ml), added Cs2CO3 (4.29 mmol), BOC2O (4.29 mmol) and stirred at rt for 16 h. The crude mixture was treated with water (150 mL) and extracted with EtOAc (3×100 mL). The combined organic phases were washed with H2O (2×50 mL), brine (2×50 mL), dried over Na2SO4, filtered and concentrated in vacuo. The product was purified by flash chromatography on silica using EtOAc in heptane as eluent.

Aufarbeitung

  1. extractionextracted with EtOAc (3×100 mL)
  2. washThe combined organic phases were washed with H2O (2×50 mL), brine (2×50 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe product was purified by flash chromatography on silica

Quellen und Nachweise

ORD-Eintrag
ord-684782151efb44a2b30e4f105d6c5583
Quelldatensatz
uspto-grants-2016_01
Patentnummer
US09233964B2

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