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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407235생성일: 2026년 10월 23일

Acetonitrile → HCID 86675410, 화합물

https://huagongshe.com/ko/reaction/407235

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium FluorideHCID 522689—
반응물4-Formylphenylboronic acid pinacol esterHCID 2769536—
반응물Methyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinateHCID 86675409—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물HCID 86675410HCID 8667541065%

반응 단계

To a 5-mL microwave safe vial was added methyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinate (0.400 g, 1.705 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (0.435 g, 1.875 mmol), KF (0.297 g, 5.11 mmol), and PdCl2(PPh3)2 (0.120 g, 0.170 mmol). A mixture of H2O (1 mL) and CH3CN (2 mL) was added, and the reaction vial was capped and placed in a Biotage Initiator microwave reactor for 20 min at 115° C. with external IR-sensor temperature monitoring from the side of the vessel. Upon cooling to room temperature, the reaction mixture was diluted with CH2Cl2 (25 mL) and H2O (25 mL), and the organic layer was filtered through a cotton plug. An additional extraction using EtOAc (25 mL) was combined with the CH2Cl2 and dried over Na2SO4 (50 g). Following filtration of the combined organics through a cotton plug and concentration on a rotary evaporator, the residue was purified using a Teledyne ISCO purification system with a gradient eluent system of CH2Cl2 and EtOAc to yield the title compound as a tan solid (335 mg, 65%): 1H NMR (400 MHz, CDCl3) δ 10.08 (s, 1H), 8.09 (dd, J=8.3, 1.5 Hz, 2H), 8.03-7.93 (m, 2H), 4.62 (s, 2H), 4.00 (s, 3H), 3.98 (s, 3H); 19F NMR (376 MHz, CDCl3) δ −139.69; ESIMS m/z 305 ([M+H]+), 303 ([M−H]−).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754229B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-fabb4b673fae4f1a94bf2f3bfa6e05f2
출처 메모uspto-grants-2014_06