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HRID 636173作成日:2026年10月26日

3-Bromo-1-propanol → N-(N-(3,5-Difluorophenylacetyl)-L-alaninyl]-L-phenylalanine 3-Bromopropyl Ester

https://huagongshe.com/reaction/636173

反応式

関与物質

役割名称HCID仕込み量
反応物3-Bromo-1-propanolHCID 12308—
反応物N-(N-(3,5-difluorophenylacetyl)-L-alaninyl]-L-phenylalanineHCID 22895006—
生成物N-(N-(3,5-Difluorophenylacetyl)-L-alaninyl]-L-phenylalanine 3-Bromopropyl EsterHCID 10118398—

反応手順

Following General Procedure B and using N-[N-(3,5-difluorophenylacetyl)-L-alaninyl]-L-phenylalanine (prepared by coupling N-(3,5-difluorophenylacetyl)-L-alanine (from Example B2 above) and L-phenylalanine (Aldrich) using General Procedure B) and 3-bromo-1-propanol (Aldrich), the title compound was prepared as a solid (mp=138-142° C.). The reaction was monitored by tlc (Rf=0.75 in 60% EtOAc/hexanes) and the product was purified by flash column chromatography using 60% EtOAc/hexanes as the eluent.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06191166B1
出典データセットuspto-grants-2001_02
ORD IDord-e63355599e474d75b8e0495e62fca1ae
出典メモuspto-grants-2001_02