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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 409783생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물DiisopropylethylamineHCID 81531—
반응물(S)-2-(5-hydroxy-4-(methylamino)pentyl)isoindoline-1,3-dioneHCID 57947589—
반응물(2-Chloro-3-fluorophenyl)methanamine hydrochlorideHCID 66622557—
생성물(S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylureaHCID 5794735947%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759374B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-7ab9cb5912614b078c4d521bfcac1682
출처 메모uspto-grants-2014_06