Reaktion #2317477

Reaktionsgleichung

product

(R)-2-Amino-3-(4-benzyloxy-phenyl)-propionic acid tert-butyl ester

product

(S)-2-[(Azepane-1-carbonyl)-amino]-4-methyl-pentanoic acid

triethylamine

HBTU

→

title compound

Ausbeute 79.8%

2(R)-{2(S)-[(Azepane-1-carbonyl)-amino]-4-methyl-pentanoylamino}-3-(4-benzyloxy-phenyl)-propionic acid tert-butyl ester

Ausbeute 79.8%

Lösungsmittel

acetonitrile

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.WAITto stand overnight
2. 2
   EinengenThe reaction mixture was concentrated
3. 3
   workup.DISSOLUTIONthe residue dissolved in ethyl acetate (100 mL)
4. 4
   Waschenwashed sequentially with 0.6 M aqueous NaHCO3 solution, saturated aqueous NaCl solution, and water
5. 5
   TrocknenThe organic phase was dried over MgSO4 and activate charcoal
6. 6
   Filtrationfiltered
7. 7
   Einengenconcentrated
8. 8
   SonstigeThe residue was purified by chromatography (silica gel, 25% ethyl acetate/hexane)

Vorschrift

A solution of the product from Example Z ((S)-2-[(azepane-1-carbonyl)-amino]-4-methyl-pentanoic acid) (0.8 g, 3.1 mmol) and triethylamine (1.6 mL, 6.2 mmol) HBTU (1.3 g, 3.4 mmol) in acetonitrile (15 mL) was treated with HBTU (1.54 g, 4.06 mmol). The resulting solution was treated with the product from Example B ((R)-2-amino-3-(4-benzyloxy-phenyl)-propionic acid tert-butyl ester) (1.08 g, 3.30 mmol), and the resulting solution was stirred at room temperature for 30 minutes and allowed to stand overnight. The reaction mixture was concentrated and the residue dissolved in ethyl acetate (100 mL) and washed sequentially with 0.6 M aqueous NaHCO3 solution, saturated aqueous NaCl solution, and water. The organic phase was dried over MgSO4 and activate charcoal, filtered, and concentrated. The residue was purified by chromatography (silica gel, 25% ethyl acetate/hexane) to give the title compound as a white solid (1.4 g, 79%), mp=38-40° C.

Quelle