Iodoethane → (S)-methyl 2-(tert-butoxycarbonyl(ethyl)amino)propanoate

(S)-methyl 2-(tert-butoxycarbonylamino)propanoate (10.0 g, 49.2 mmol) was dissolved in THF (100 mL) and cooled to 0° C. under nitrogen. Sodium hydride (60% susp. in mineral oil, 3.00 g, 75.1 mmol) was added in portions over 2 min. The reaction mixture was stirred for 5 min at 0° C. and EtI (4.80 mL, 59.5 mmol) was added. It was allowed to warm to room temperature over the period of 1 h, stirred at room temperature overnight and at 70° C. for 7 d. The reaction mixture was cooled, filtered and concentrated in vacuo. The solid was triturated with hexanes (2×70 mL), the triturates were concentrated in vacuo and the residue was purified using flash column chromatography on silica gel (330 g SiO2, hexanes:ethyl acetate 19:1-9:1) to afford the title compounds as an oil (4.40 g, 39%). [M+H] calc'd for C11H21NO4, 232; found, 232.

1. temperatureto warm to room temperature over the period of 1 h
2. stirringstirred at room temperature overnight and at 70° C. for 7 d
3. temperatureThe reaction mixture was cooled
4. filtrationfiltered
5. concentrationconcentrated in vacuo
6. customThe solid was triturated with hexanes (2×70 mL)
7. concentrationthe triturates were concentrated in vacuo
8. customthe residue was purified

ORD-Eintrag

ord-78d922a22f9c4e1bb1c36f950ec9e1d4

Quelldatensatz

uspto-grants-2012_02

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08124606B2