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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32662생성일: 2026년 10월 24일

Tetrahydrofuran → 3-[4-(4-Acetyl-2-fluoro-phenyl)-piperazine-1-carbonyl]-4-azepan-1-yl-benzonitrile

https://huagongshe.com/ko/reaction/32662

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물AzepaneHCID 8119—
반응물DiisopropylethylamineHCID 81531—
반응물3-[4-(4-Acetyl-2-fluoro-phenyl)-piperazine-1-carbonyl]-4-bromo benzonitrileHCID 59793521—
용매DimethylformamideHCID 6228—
생성물3-[4-(4-Acetyl-2-fluoro-phenyl)-piperazine-1-carbonyl]-4-azepan-1-yl-benzonitrileHCID 59793714—

반응 조건

온도100 °C

반응 단계

A mixture of 30.1 mg (0.7 mmol) 3-[4-(4-Acetyl-2-fluoro-phenyl)-piperazine-1-carbonyl]-4-bromo-benzonitrile, 30 ul (0.175 mmol) DIPEA and 91 ul (0.91 mmol) of a 1M solution of azepane in DMF was heated to 100° C. for 24 h. After removal of THF 2 ml dioxane, 180 ul of a 1M solution of azepane in DMF and 30 ul (0.175 mmol) DIPEA were added and the mixture was heated to 120° C. for 16 h. After evaporation of all volatiles the residue was taken up in 1 ml MeOH/formic acid 6/1 and subjected to reversed phase HPLC purification eluting with an acetonitrile/water gradient to yield after evaporation of the product fractions 9.3 mg (30%) of the title compound. MS (m/e): 449.2 (MH+, 100%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427612B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-a57e187189634134a1f8a34fd3c57b41
출처 메모uspto-grants-2008_09