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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 610126생성일: 2026년 10월 25일

Sodium Carbonate → 2-[Bis(tert-butoxycarbonyl)amino]-5-(2'-methylthiophenyl)pyrimidine

https://huagongshe.com/reaction/610126

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-(Methylthio)benzeneboronic acidHCID 2773543—
반응물tert-butyl N-(5-bromopyrimidin-2-yl)-N-((tert-butoxy)carbonyl)carbamateHCID 11977091—
촉매Tetrabutylammonium BromideHCID 74236—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매BenzeneHCID 241—
생성물2-[Bis(tert-butoxycarbonyl)amino]-5-(2'-methylthiophenyl)pyrimidineHCID 1817732096.3%

반응 단계

2-[Bis(tert-butoxycarbonyl)amino]-5-bromopyrimidine (2.00 g, 5.3 mmol) was dissolved in benzene (130 mL). 2-methylthiophenylboronic acid (2.24 g, 13.3 mmol), aq. sodium carbonate (13 mL, 2.0 M, 26 mmol), tetrabutyl ammonium bromide (86 mg, 0.26 mmol), and bis(triphenylphosphine)palladium(II)chloride (190 mg, 0.27 mmol) were added, and the resulting mixture was first purged with vacuum and argon, then refluxed 17 hours. The cooled mixture was diluted with EtOAc and water. The layers were separated, and the organic was dried over Na2SO4, filtered, and evaporated. The crude product was chromatographed on silica gel (50% EtOAc/hexanes), evaporated, and chromatographed a second time on silica gel (30-50% EtOAc/hexanes) to yield the desired product (2.13 g, 96%). 1H NMR (CDCl3): δ8.81 (s, 2H) , 7.41 (m, 2H) , 7.25 (m, 2H) , 2.39 (s, 3H), 1.49 (s, 18H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05998424
출처 데이터셋uspto-grants-1999_12
ORD IDord-8f82250f3e6b46f1be227e7a0ed79668
출처 메모uspto-grants-1999_12