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HRID 409783作成日:2026年10月24日

Tetrahydrofuran → (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea

https://huagongshe.com/ja/reaction/409783

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物DiisopropylethylamineHCID 81531—
反応物(S)-2-(5-hydroxy-4-(methylamino)pentyl)isoindoline-1,3-dioneHCID 57947589—
反応物(2-Chloro-3-fluorophenyl)methanamine hydrochlorideHCID 66622557—
生成物(S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylureaHCID 5794735947%

反応手順

To a solution of 4-nitrophenylchloroformate (460 mg, 2.29 mmol) in THF (20 mL) was added 2-chloro-3-fluorobenzylamine hydrochloride (626 mg, 2.29 mmol) and DIEA (0.76 mL, 4.58 mmol) and the mixture was stirred at RT until TLC showed complete consumption of 2-chloro-3-fluorobenzylamine. The mixture was then added into a solution of (S)-2-(5-hydroxy-4-(methylamino)pentyl)isoindoline-1,3-dione (500 mg, 1.91 mmol) in THF (10 mL). The mixture was stirred overnight, concentrated and purified on RP-HPLC using a mixture of acetonitrile and H2O to give (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea (401 mg, 47%). LRMS (M+H+) m/z 448.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759374B2
出典データセットuspto-grants-2014_06
ORD IDord-7ab9cb5912614b078c4d521bfcac1682
出典メモuspto-grants-2014_06