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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 474141생성일: 2026년 10월 24일

Potassium Phosphate, Tribasic → 2-(4-(Pyrazin-2-yl)phenyl)acetic acid

https://huagongshe.com/ko/reaction/474141

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물IodopyrazineHCID 642841—
반응물2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetic AcidHCID 3719002—
촉매TricyclohexylphosphineHCID 75806—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물2-(4-(Pyrazin-2-yl)phenyl)acetic acidHCID 5953593832%

반응 단계

To a solution of 0.40 g (1.53 mmol) of [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetic acid in 4.0 ml of dioxane was added 0.18 mL (1.73 mmol) of 2-iodopyrazine, 10.3 mg (0.037 mmol) of tricyclohexylphosphine, 13.9 mg (0.015 mmol) of Pd2(dba)3, and 2.0 ml (1.27 M, 2.59 mmol) of aqueous potassium phosphate solution. The resulting suspension was degassed for 10 mins. After 30 min in the microwave at 150° C., the reaction mixture was cooled, acidified with 1N HCl, extracted with ethyl acetate, and washed with brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. Purification by preparative HPLC (5->95% CH3CN/H2O over 15 min, 0.05% added TFA, C18) afforded 0.10 g (32%) of (4-pyrazin-2-ylphenyl)acetic acid. 1H NMR (CD3OD, 400 MHz) 9.1 (s, 1H); 8.66 (t, J=1.74 Hz, 1H); 8.51 (d, J=2.57 Hz, 1H); 8.04 (d, J=8.15 Hz, 2H); 7.46 (d, J=8.15 Hz, 2H); 3.70 (s, 2H). ES-MS M+1=215.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637513B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-cec6615b53614e45a6d4766dc3e42e06
출처 메모uspto-grants-2014_01