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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79112생성일: 2026년 10월 24일

3-Chloro-4-pyridineboronic acid → 5-(3-Chloro-pyridin-4-yl)-N4-(tetrahydro-pyran-4-yl)-pyrimidine-2,4-diamine

https://huagongshe.com/ko/reaction/79112

반응식

참여 물질

역할이름HCID투입량
반응물3-Chloro-4-pyridineboronic acidHCID 3861877—
반응물5-Bromo-N4-(tetrahydro-pyran-4-yl)-pyrimidine-2,4-diamineHCID 58299673—
촉매HCID 178418476HCID 178418476—
용매1,4-DioxaneHCID 31275—
생성물5-(3-Chloro-pyridin-4-yl)-N4-(tetrahydro-pyran-4-yl)-pyrimidine-2,4-diamineHCID 5830002198%

반응 조건

온도130 °C

반응 단계

A mixture of compound 33 (2.03 g, 7.43 mmol), 3-chloropyridin-4-ylboronic acid (3.51 g, 22.3 mmol), and Pd(PPh3)2Cl2 (0.522 g, 0.743 mmol) in dioxane (44 ml) in a pressure vessel was purged with N2 for 20 minutes and to this mixture was added aq. Na2CO3 (1 M, 22 mL) by syringe. The reaction was further purged with N2 for another 20 minutes and then heated to 130° C. for 12 hours. DCM was added to the reaction and the mixture was washed with water and brine. The organic layer was dried with sodium sulfate and concentrated to provide compound 34 (2.07 g, crude, 98%) which was used in the next reaction without further purification. LCMS-ESI (POS), M/Z, M+1: Found 306.1, Calculated 306.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841312B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-633972e782a343608819f24c9088577b
출처 메모uspto-grants-2014_09