Sodium Hydroxide → Ethyl (2R,6S,12Z,13aS,14aR,16aS)-6-({[(2,2-dimethylpent-4-en-1-yl)oxy]carbonyl}amino)-2-[(6-methoxy-7-vinylisoquinolin-1-yl)oxy]-5,16-dioxo-1,2,3,6,7,8,9,10,11,13a,14,15,16,16a-tetradecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecine-14a(5H)-carboxylate

To a stirred solution of 2,2-dimethylpent-4-en-1-ol (66.3 mg, 0.581 mmol) and DIPEA (0.101 mL, 0.581 mmol) in anhydrous 1,4-dioxane (10 mL), at 10° C., under nitrogen, was added a solution of triphosgene (60.3 mg, 0.203 mmol) in 1,4-dioxane (10 mL). The reaction mixture was stirred at RT for 1 hour. The product from Step 6 (178 mg, 0.290 mmol) and 1 M NaOH (0.871 mL) were then added and the reaction mixture was stirred at 50° C. for 15 hours. The reaction mixture was cooled to RT, diluted with aqueous saturated NaHCO3 (20 mL) and extracted with EtOAc (3×30 mL). The combined EtOAc layers were washed with water (30 mL), brine (20 mL), dried over Na2SO4, filtered and concentrated. The residue was chromatographed on silica gel, eluting with 5% to 75% EtOAc in hexane, to give the title product (125 mg). LRMS (ESI) m/z 717.5 [(M+H)+; calcd for C40H53N4O8: 717.4].

1. stirringthe reaction mixture was stirred at 50° C. for 15 hours
2. temperatureThe reaction mixture was cooled to RT
3. extractionextracted with EtOAc (3×30 mL)
4. washThe combined EtOAc layers were washed with water (30 mL), brine (20 mL)
5. dry with materialdried over Na2SO4
6. filtrationfiltered
7. concentrationconcentrated
8. customThe residue was chromatographed on silica gel
9. washeluting with 5% to 75% EtOAc in hexane

ORD-Eintrag

ord-6ba04cd58b0349b88b7eeea3af1bf5ff

Quelldatensatz

uspto-grants-2013_02

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08377874B2