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HRID 7436作成日:2026年10月23日

t-Butyl 2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetate → 2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetic acid

https://huagongshe.com/ja/reaction/7436

反応式

関与物質

役割名称HCID仕込み量
反応物t-Butyl 2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetateHCID 9912947—
溶媒Trifluoroacetic acid methylene chlorideHCID 21863450—
生成物2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetic acidHCID 2199053782.9%

反応手順

t-Butyl 2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetate (210 mg, 0.4 mmol) was dissolved in trifluoroacetic acid-dichloromethane (4:1, 2 mL) and the mixture was stirred at room temperature for 15 min. The reaction mixture was concentrated under reduced pressure and the precipitated crystals were recrystallized from ethyl acetate to give the title compound (140 mg, 70%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087597B1
出典データセットuspto-grants-2006_08
ORD IDord-f6f742a697e84fcea25f99e5bc06f882
出典メモuspto-grants-2006_08