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HRID 391789作成日:2026年10月24日

Boc-Tyr-OMe → (S)-2-tert-Butoxycarbonylamino-3-[4-(2,3-dimethyl-pyridin-4-yloxy)-phenyl]-propionic acid methyl ester

https://huagongshe.com/ja/reaction/391789

反応式

関与物質

役割名称HCID仕込み量
反応物Boc-Tyr-OMeHCID 7019130—
反応物Water ethylacetateHCID 22728543—
反応物(2,3-Dimethylpyridin-4-YL)boronic acidHCID 58327508—
溶媒DichloromethaneHCID 6344—
生成物(S)-2-tert-Butoxycarbonylamino-3-[4-(2,3-dimethyl-pyridin-4-yloxy)-phenyl]-propionic acid methyl esterHCID 583272604.4%

反応手順

A mixture of 304 mg of (S)-2-tert-butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionic acid methyl ester, 314 mg 2,3-dimethylpyridine-4-boronic acid, 374 mg cupric acetate, and 2 grams of powdered 4 Å molecular seives in 50 mL dry DCM and 0.75 mL TEA was stirred vigorously at rt under an O2 atmosphere for 40 h. The mixture was then poured into water-EtOAc. The organic layer was washed with water and saturated brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (DCM-EtOAc) to provide (S)-2-tert-Butoxycarbonylamino-3-[4-(2,3-dimethyl-pyridin-4-yloxy)-phenyl]-propionic acid methyl ester (18 mg). LCMS (m/z) 401.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383644B2
出典データセットuspto-grants-2013_02
ORD IDord-20f9e83aab2a44b48e438a2896fa247a
出典メモuspto-grants-2013_02