돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 82280생성일: 2026년 10월 24일

Triethylamine → (5-Bromo-2-chloro-pyrimidin-4-yl)-(2-methoxy-1,1-dimethyl-ethyl)-amine

https://huagongshe.com/ko/reaction/82280

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물PyrimidineHCID 9260—
반응물1-Methoxy-2-methylpropan-2-amineHCID 88666—
반응물5-Bromo-2,4-dichloropyrimidineHCID 289973—
용매AcetonitrileHCID 6342—
생성물(5-Bromo-2-chloro-pyrimidin-4-yl)-(2-methoxy-1,1-dimethyl-ethyl)-amineHCID 8667212423%

반응 단계

Triethyl amine (73.1 mL, 526.6 mmol) was added slowly to a solution of 5-Bromo-2,4-dichloro-pyrimidine (40 g, 175.5 mmol) in acetonitrile (400 mL) at 00° C. and then 2-Methoxy-1,1-dimethyl-ethylamine (Preparation 255, 23.4 g, 263.3 mmol) was added to the mixture portion wise. The reaction mixture was stirred for another 16 hours at room temperature. TLC showed the presence of unreacted starting pyrimidine, but the reaction was not continued further. All the volatiles were removed in vacuo and the residue was taken in ethyl acetate, washed with water, brine, dried over sodium sulphate and evaporated to dryness in vacuo. The crude material was purified by column chromatography on silica gel (100-200 mesh, gradient of ethyl acetate:hexane 1:9 to 2:4) to afford the title compound as white solid in 23% yield (10 g of starting pyrimidine was recovered), 12 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846698B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b8b92e1d45b34c79bf8e55407ea18755
출처 메모uspto-grants-2014_09