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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219476생성일: 2026년 10월 25일

3-Hydroxyazetidine hydrochloride → 1-[3-Chloro-6-[2-(3-hydroxy-azetidin-1-yl)-ethoxy]-4-methoxy-2-methyl-5-(3-phenyl-propoxy)-phenyl]-ethanone

https://huagongshe.com/reaction/219476

반응식

참여 물질

역할이름HCID투입량
반응물3-Hydroxyazetidine hydrochlorideHCID 2759290—
반응물1-[2-(2-Bromo-ethoxy)-5-chloro-4-methoxy-6-methyl-3-(3-phenyl-propoxy)-phenyl]-ethanoneHCID 59583495—
생성물1-[3-Chloro-6-[2-(3-hydroxy-azetidin-1-yl)-ethoxy]-4-methoxy-2-methyl-5-(3-phenyl-propoxy)-phenyl]-ethanoneHCID 2525437316%

반응 단계

Example 34b (207 mg, 0.46 mmol), CsCO3 (2.48 eq.) and 3-hydroxyazetidine hydrochloride (1.4 eq.) were reacted as described under General Procedure L and the crude product was purified by flash chromatography (silica gel, hexane/Et2O 1:1) to afford the title compound as a pale yellow oil (34 mg, 16%). 1H NMR (300 MHz, CDCl3) δ 7.33-7.20 (m, 5H), 4.40 (quintet, J=5.7 Hz, 1H), 4.07 (t, J=6.5 Hz, 2H), 3.98 (t, J=5.7 Hz, 2H), 3.88 (s, 3H), 3.67-3.62 (m, 2H), 2.96-2.91 (m, 2H), 2.85-2.80 (m, 2H), 2.73 (t, J=5.7 Hz, 2H), 2.51 (s, 3H), 2.19 (s, 3H), 2.13-2.03 (m, 2H). MS (ES+) m/z 448.2 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202513B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-ea511563eaac4a8eb94add805345610e
출처 메모uspto-grants-2012_06