Реакция #89651
ord-9e542c44bc924576a853d4ac124a19a3
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1Температураcooled to room temperature
- 2workup.STIRRINGstirred for 18 h
- 3workup.STIRRINGthe mixture stirred for a few minutes
- 4Экстракцияextracted with ethyl acetate (30 mL
- 5ПромывкаThe combined organic solution was washed with water and saturated aqueous sodium chloride (20 mL each)
- 6Сушкаdried (MgSO4)
- 7Концентрированиеconcentrated
- 8Другоеisolated
Методика
A stirred solution of (3R,4S)-3-acetamido-N-tert-butyl-4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)pyrrolidine-3-carboxamide (Example 8, step 4) (198 mg, 0.5 mmol) and N-BOC-pyrrolidine-3-one (0.185 g, 1.0 mmol) in anhydrous 1,2-dichloroethane (5 mL) was treated with anhydrous sodium sulfate (1 g) and glacial acetic acid (30 mg, 0.5 mmol), stirred at 40° C. for 2.5 h, then cooled to room temperature and treated with sodium triacetoxyborohydride (276 mg, 1.3 mmol) and stirred for 18 h. Aqueous sodium carbonate (10%, 5 mL) was added and the mixture stirred for a few minutes and extracted with ethyl acetate (30 mL, then 2×10 mL). The combined organic solution was washed with water and saturated aqueous sodium chloride (20 mL each), dried (MgSO4), and concentrated. The crude material was deprotected and isolated using the method described for example 8, step 5 to afford (3R,4S)-3-amino-4-(3-boronopropyl)-1,3′-bipyrrolidine-3-carboxylic acid (160 mg, 81%) as an amber solid. NMR (D2O) δ 4.25-4.35 (m, 1 H), 4.00 (dd, J1=12 Hz, J2=5 Hz, 1 H) 3.70-3.95 (m, 3 H), 3.25-3.60 (m, 4 H), 2.45-2.65 (m, 2 H), 2.15-2.25 (m, 1 H), 1.50-1.65 (m, 1 H), 1.15-1.35 (m, 3 H), 0.60-0.70 (m, 2 H). MS (m+1): 286.1; MS (m−H2O+1): 268.3.