돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 709310생성일: 2026년 10월 26일

3-Iodophenol → (E)-tert-butyl 4-(4-(5-(3-hydroxystyryl)pyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/709310

반응식

참여 물질

역할이름HCID투입량
반응물3-IodophenolHCID 12272—
반응물Phosphine, tris(4-methylphenyl)-HCID 13956—
반응물DiisopropylethylamineHCID 81531—
반응물Tert-butyl 4-(4-(5-vinylpyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylateHCID 67324584—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물(E)-tert-butyl 4-(4-(5-(3-hydroxystyryl)pyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylateHCID 6732568878.5%

반응 조건

온도120 °C

반응 단계

A mixture of tert-butyl 4-(4-(5-vinylpyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylate (40 mg, 0.09 mmol), 3-iodophenol (19 mg, 0.09 mmol), Pd(OAc)2 (1.2 mg, 0.005 mmol), tri-p-tolylphosphine (2.5 mg, 0.008 mmol), and DIEA (31 μL, 0.18 mmol) in DMF (3 ml) was heated at 120° C. for 18 h after which, it was filtered with a pad of celite and partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, celite filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography using (20% to 40% Ethyl acetate/Hexane) as a solvent to afford title compound (38 mg, 78% yield). MS m/z: 538 [M+1].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09180127B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-4c6951e557ba4a1cb8027db3defda424
출처 메모uspto-grants-2015_11