反应详情

Prepared using General Procedure 7: A stirred solution of (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-(5-(4-(heptyloxy)phenyl)pyrimidin-2-yl)phenyl) propanoic acid INT-22 (1 g, 1.76 mmol), tert-butyl azetidine-3-carboxylate (0.554 g, 1.76 mmol) and DIEA (1.30 mL, 7.05 mmol) in DMF (20 mL) at 0° C. was treated with HATU (0.703 g, 1.85 mmol), added portionwise. After 10 min, the cooling bath was removed. After a further 1 h the mixture was poured onto 0.2 M HCl (100 mL) and extracted with EA (3×30 mL). The combined organic extracts were washed with brine (20 mL), dried over MgSO4 and evaporated. Column chromatography (EA/DCM/iso-hexanes) gave 708 mg (58%) often-butyl (S)-1-(2-(((benzyloxy)carbonyl)amino)-3-(4-(5-(4-(heptyloxy)phenyl)pyrimidin-2-yl)phenyl)propanoyl)azetidine-3-carboxylate as an off-white solid. LCMS-ESI (m/z) calculated for C42H50N4O6: 706.4. found 707.1 [M+H]+, tR=3.60 min (Method 6).

1. customPrepared
2. additionadded portionwise
3. customthe cooling bath was removed
4. additionAfter a further 1 h the mixture was poured onto 0.2 M HCl (100 mL)
5. extractionextracted with EA (3×30 mL)
6. washThe combined organic extracts were washed with brine (20 mL)
7. dry with materialdried over MgSO4
8. customevaporated