돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68652생성일: 2026년 10월 24일

Potassium Phosphate, Tribasic → 5-(4-(Isopropylsulfonyl)phenyl)pyrazin-2-amine

https://huagongshe.com/ko/reaction/68652

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-Amino-5-bromopyrazineHCID 599539—
반응물4-(Isopropylsulphonyl)benzeneboronic acidHCID 44119327—
촉매HCID 178418851HCID 178418851—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물5-(4-(Isopropylsulfonyl)phenyl)pyrazin-2-amineHCID 5808438280.7%

반응 조건

온도60 °C

반응 단계

5-Bromopyrazin-2-amine (5 g, 28.74 mmol), (4-isopropylsulfonylphenyl) boronic acid (7.866 g, 34.49 mmol) and K3PO4 (12.20 g, 57.48 mmol) were combined in MeCN (100 mL)/Water (25 mL) and Pd[P(tBu)3]2 (734.4 mg, 1.437 mmol) was added. The reaction was heated at 60° C. for 1 hour. The reaction mixture was cooled to ambient temperature and diluted with EtOAc and water. The layers were separated and the aqueous layer extracted with EtOAc (×3). The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo. The residue was triturated from DCM and isolated by filtration to give the sub-title compound as an orange solid (6.43 g, 76% Yield). 1H NMR (400.0 MHz, DMSO) δ 1.17 (d, 6H), 3.43 (sept, 1H), 6.86 (s, 2H), 7.87 (d, 2H), 8.00 (s, 1H), 8.20 (d, 2H) and 8.67 (s, 1H) ppm; MS (ES+) 278.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822469B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-61a69da484c1490a8b1889e647c37046
출처 메모uspto-grants-2014_09