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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1044408생성일: 2026년 10월 26일

Pyridine → 4-chloro-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyridin-2(1H)-one

https://huagongshe.com/reaction/1044408

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-Chloropyridin-2-olHCID 2757611—
반응물4-(2-Hydroxy-2-methylpropoxy)-3-methoxyphenylboronic acidHCID 58579863—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물4-chloro-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyridin-2(1H)-oneHCID 5858029462.8%

반응 단계

Pyridine (1.2 mL, 15.4 mmol) was added to a stirred solution of commercially available 4-chloropyridin-2(1H)-one (100 mg, 0.77 mmol), 4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenylboronic acid Part C (278 mg, 1.16 mmol), and copper (II) acetate, monohydrate (154 mg, 0.77 mmol) in CH2Cl2 (7 mL) and MeOH (0.7 mL). The reaction mixture stirred at RT under the presence of air overnight (21 hours). The reaction mixture was diluted with CH2Cl2, washed with IN HCl, sat. NaHCO3, dried (Na2SO4), and concentrated. The crude product was purified using preparative HPLC (C18 column/10:90:0.1 to 90:10:0.1 MeOH—H2O-TFA) to afford the desired product 4-chloro-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyridin-2(1H)-one 9D (169 mg, 0.49 mmol, 62.8% yield) as a brown gum. LC/MS 324 (M+H)+, tR 0.75 min (method 5)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08563583B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-febe04c268f74042b1c1e8a49da96f38
출처 메모uspto-grants-2013_10