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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 410380생성일: 2026년 10월 25일

Potassium Fluoride → HCID 58456408, 화합물

https://huagongshe.com/reaction/410380

반응식

참여 물질

역할이름HCID투입량
반응물Potassium FluorideHCID 522689—
반응물5-BromothiazoleHCID 546059—
반응물Bis(adamantan-1-yl)(butyl)phosphaneHCID 11371790—
반응물HCID 58456329HCID 58456329—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물HCID 58456408HCID 5845640866%

반응 조건

온도75 °C

반응 단계

A solution of Pd(OAc)2 (19 mg, 0.085 mmol) and butyl di-1-adamantyl phosphine (61 mg, 0.18 mmol) in THF (12.8 mL) was stirred for 15 min. Intermediate 10 (755 mg, 1.70 mmol), 5-bromo-1,3-thiazole (760 μL, 8.50 mmol), potassium fluoride (296 mg, 5.10 mmol), and water (4.25 mL) were then added, and the mixture was heated to 75° C. overnight. After cooling to rt, the mixture was diluted with 100 mL EtOAc and washed with 100 mL brine. A bright yellow solid remained undissolved on the walls of the separatory funnel, which was thus rinsed with 100 mL THF. The combined organic extracts were dried (Na2SO4) and concentrated in vacuo. Purification by Chromatography on silica gel (40 g; dry load; 100:0 to 50:50 hexanes:EtOAc over 25 minutes) provided N-[3-bromo-5-(1,3-thiazol-5-yl)phenyl]-4-(trifluoromethyl)pyrimidin-2-amine (449 mg, 1.12 mmol, 66%) as an off-white solid. MS APCI: [M+H]+ m/z 403.0. 1H NMR (400 MHz, (CD3)2CO): δ 9.46 (s, 1H); 9.03 (s, 1H); 8.89 (d, J=4.9 Hz, 1H); 8.32-8.26 (m, 2H); 8.16 (s, 1H); 7.59 (s, 1H); 7.33 (d, J=4.9 Hz, 1H). rhSYK activity=++.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759366B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-6a54562f302948d4b0771acc6648bff8
출처 메모uspto-grants-2014_06