돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 593774생성일: 2026년 10월 25일

1,4-Dioxane → 4-(Benzo[b]thiophen-7-yl)isoquinoline

https://huagongshe.com/reaction/593774

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Isoquinoline-4-boronic acidHCID 3761204—
반응물7-Bromobenzo[b]thiopheneHCID 12045538—
촉매HCID 178418807HCID 178418807—
용매DichloromethaneHCID 6344—
생성물4-(Benzo[b]thiophen-7-yl)isoquinolineHCID 8673043030%

반응 조건

온도90 °C

반응 단계

A vessel capable of sealing was charged with a mixture of 7-bromobenzo[b]thiophene (430 mg, 2.018 mmol), isoquinolin-4-ylboronic acid (419 mg, 2.421 mmol), PdCl2(dppf)-CH2Cl2 adduct (82 mg, 0.101 mmol), dioxane (6 mL), and a 2.0 M aqueous solution of K3PO4 (3 mL, 1.41 mmol) and was purged with nitrogen for 10 min. The vessel was sealed and heated at 90° C. for 16 hours. Upon cooling, the reaction mixture was diluted with CH2Cl2 and filtered with CH2Cl2/MeOH washing. The filtrate was concentrated under reduced pressure. The residue was dissolved in CH2Cl2 and washed with water, brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude material was purified by BIOTAGE® eluting with 0%-15% EtOAc/CH2Cl2 at 30 mL/min. Concentration of appropriate fractions provided the title compound (32 mg, 30% yield). LC/MS: Example 109A @ 2.49 min (RT) (Condition G). MS (ES): m/z=262.42 [M+H]+. 1H NMR (400 MHz, CDCl3) δ ppm 9.38 (1 hr, s), 8.71 (1 hr, s), 8.08-8.15 (1 hr, m), 7.96 (1 hr, dd, J=8.06, 1.01 Hz), 7.51-7.71 (4 hr, m), 7.39-7.51 (3 hr, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242967B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-bcd3bf51ef9f45489778d55081e9fe55
출처 메모uspto-grants-2016_01