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HRID 1913315作成日:2026年10月25日

Dimethylformamide → Methyl (S)-2-benzyloxycarbonylamino-3-chlorocarbonylpropionate

https://huagongshe.com/reaction/1913315

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物Z-Asp-OMeHCID 7021783—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl (S)-2-benzyloxycarbonylamino-3-chlorocarbonylpropionateHCID 11055664—

反応手順

Z-asp-OMe (175 g, 622 mmol) was dissolved in THF (1750 ml) and admixed with 2 ml of DMF. 86.9 g (684 mmol) of oxalyl chloride were dissolved in 200 ml of THF (slightly exothermic), cooled back to room temperature (RT) and added dropwise to the solution of the amino acid over 1 hour (h). After a further hour at RT, the solution was initially sparged with nitrogen for 10 min, concentrated on a rotary evaporator at a maximum of 30° C. and coevaporated repeatedly with toluene. The resulting dirty white solid was dried to constant weight under in-house vacuum (about 1.5 mbar) and reacted further without further purification. Yield: 186.6 g (quantitative).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08609681B2
出典データセットuspto-grants-2013_12
ORD IDord-231b7b358c8d4d6b82149181a3dfba60
出典メモuspto-grants-2013_12