Methyl iodide → HCID 57270309, Verbindung

Temperatur

0 °C

A THF solution of sodium bis(trimethylsily)amide (0.059 mL, 1.0M, 0.059 mmol) was added to an ice-cooled solution of (3S,5R,6R,7S)-7-(benzyloxycarbonylamino)-6-(4-fluorophenyl)-3-(2-methoxy-5-(2-(trifluoromethyl)imidazol-1-yl)phenyl)-1-oxaspiro[4.4]nonane (30 mg, 0.049 mmol) in 0.50 mL of dry THF. After stirring for 15 minutes at 0° C., iodomethane (0.0037 mL, 8.4 mg, 0.059 mmol) was added. The mixture was stirred at 0° C., then allowed to warm up to RT for 3 h. The reaction was diluted in 20 mL of ethyl acetate and washed with 10 mL of saturated aqueous sodium bicarbonate, followed by 10 mL of brine. Drying over sodium sulfate and concentration afforded the crude product. Purification by preparative TLC, eluting with 30% ethyl ether in 1:1 toluene/hexane, yielded 7.5 mg of pure title compound and 15 mg of a mixture containing the title compound and recovered starting material. Mass spectrum (NH3/CI): m/z=624.2 (M+1).

1. stirringThe mixture was stirred at 0° C.
2. temperatureto warm up to RT for 3 h
3. washwashed with 10 mL of saturated aqueous sodium bicarbonate
4. dry with materialDrying over sodium sulfate and concentration
5. customafforded the crude product
6. customPurification by preparative TLC
7. washeluting with 30% ethyl ether in 1:1 toluene/hexane

ORD-Eintrag

ord-fd1ef373e2cd4d4ba1e33f89a23b3c8d

Quelldatensatz

uspto-grants-1999_03

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05877191