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HRID 58852作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/58852

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物TriphenylphosphineHCID 11776—
反応物Iodide IonHCID 30165—
反応物N-((Phenylmethoxy)carbonyl)-L-serine methyl esterHCID 6999535—
溶媒DichloromethaneHCID 6344—
生成物(R)-2-Benzyloxycarbonylamino-3-iodo-propionic acid methyl esterHCID 1091543757%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434761B2
出典データセットuspto-grants-2016_09
ORD IDord-b7080d56f1c34e4f836b16936cfd75d5
出典メモuspto-grants-2016_09