反应详情

温度

30 °C

To a solution of (3S*,4R*)-3-benzylcarbamoyl-4-({isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (61 mg, 0.098 mmol) in 2 mL CH2Cl2, TFA (113 μL, 1.46 mmol) is added. The mixture is stirred at 30° C. for 2 h, then overnight at RT, and poured into a saturated solution of NaHCO3. The layers are separated, and the aqueous one is back-extracted twice with CH2Cl2. The combined organic extracts are dried over Na2SO4, filtered and concentrated. The crude material is purified by flash chromatography on an NH2 Isolute SPE Flash column (eluent: CH2Cl2:MeOH 100:0 to 95:5) to give the title product. TLC, Rf (CH2Cl2/MeOH 9:1)=0.2. MS (LC-MS): 498 [M+H]+; tR (HPLC, Nucleosil C18 column, 10-100% CH3CN/H2O/5 min, 100% CH3CN/3 min, CH3CN and H2O containing 0.1% TFA, flow: 1.5 mL/min): 4.38 min.

1. customThe layers are separated
2. extractionthe aqueous one is back-extracted twice with CH2Cl2
3. dry with materialThe combined organic extracts are dried over Na2SO4
4. filtrationfiltered
5. concentrationconcentrated
6. customThe crude material is purified by flash chromatography on an NH2 Isolute SPE Flash column (eluent: CH2Cl2:MeOH 100:0 to 95:5)