Reaktion #1838260

Reaktionsgleichung

tert-butyl 3-((1-cyclohexyl-8-(4-(4-fluorophenyl)-4-oxobutyl)-4-oxo-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate

hydrochloric acid

→

product

Ausbeute 75.0%

3-((1-cyclohexyl-8-(4-(4-fluorophenyl)-4-oxobutyl)-4-oxo-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoic acid, hydrochloride

Ausbeute 75.0%

Lösungsmittel

1,4-dioxane

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe reaction was evaporated
2. 2
   Sonstigethe residue purified by PTLC (10% methanol/dichloromethane)
3. 3
   workup.DISSOLUTIONwas redissolved in 4M hydrochloric acid in dioxane
4. 4
   Sonstigeevaporated
5. 5
   workup.DISSOLUTIONThe residue was dissolved in acetonitrile (5 mL)

Vorschrift

tert-butyl 3-((1-cyclohexyl-8-(4-(4-fluorophenyl)-4-oxobutyl)-4-oxo-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate (0.39 g, 0.659 mmol) and 4M hydrochloric acid/1% triethylsilane in 1,4-dioxane (6 mL) were stirred at room temperature for 4 hours. The reaction was evaporated and the residue purified by PTLC (10% methanol/dichloromethane). The product obtained from PTLC was redissolved in 4M hydrochloric acid in dioxane and evaporated. The residue was dissolved in acetonitrile (5 mL) and water (5 mL) and lyophilized to give product as a white solid (0.28 g, 75%); HPLC rt 10.92 min; NMR (DMSO-d6); δ1.02-1.08 (m, 1H); 1.18-1.28 (m, 4H); 1.28-1.40 (m, 1H); 1.45-1.65 (m, 2H); 1.65-1.78 (m, 3H); 1.85-2.10 (m, 3H); 2.33-2.50 (m, 2H); 3.10 (m, 2H); 3.22 (t, J=6.8 Hz, 2H); 3.49-3.56 (m, 5H); 4.52 (s, 2H); 7.35-7.40 (m, 2H); 7.50 (m, 2H); 7.85-7.86 (m, 2H); 8.05-8.09 (m, 2H); 10.6 (br s, 1H); 13.0 (br s, 1H); MS for C31H38FN3O4 m/z 536 (M+H)+.

Quelle