Imidazole → (R)-2-Benzyloxycarbonylamino-3-iodo-propionic acid methyl ester

温度

0 °C

A mixture of triphenylphosphine (23.3 g, 0.890 mol) and imidazole (6.0 g, 0.89 mol) in DCM (100 mL) was cooled to 0° C. and iodide (22.6 g, 0.890 mol) was added in small portions over 0.5 h. The cooling bath was removed and the mixture was stirred for 0.5 h. After the mixture was re-cooled to 0° C., a solution of Cbz-L-Ser-OMe 15.0 g, 0.590 mol) in DCM (100 mL) was added dropwise. After the addition, the cooling bath was removed and the mixture was allowed to warm to ambient temperature and stirred for 1.5 h. The mixture was filtered and the filtrate was concentrated to remove most of the solvent. MTBE (400 mL) was added to the residue and the mixture was filtered to remove triphenylphosphine oxide. The filtrate was concentrated and the residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=50:1 to 10:1) to afford (R)-methyl 2-(benzyloxycarbonylamino)-3-iodopropanoate (12.3 g, 57% yield) as a colorless solid.

1. customThe cooling bath was removed
2. temperatureAfter the mixture was re-cooled to 0° C.
3. additionAfter the addition
4. customthe cooling bath was removed
5. temperatureto warm to ambient temperature
6. stirringstirred for 1.5 h
7. filtrationThe mixture was filtered
8. concentrationthe filtrate was concentrated
9. customto remove most of the solvent
10. additionMTBE (400 mL) was added to the residue
11. filtrationthe mixture was filtered
12. customto remove triphenylphosphine oxide
13. concentrationThe filtrate was concentrated
14. customthe residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=50:1 to 10:1)

ORDレコード

ord-b7080d56f1c34e4f836b16936cfd75d5

出典データセット

uspto-grants-2016_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09434761B2