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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1036779생성일: 2026년 10월 26일

3-Amino-6-chloro-4-picoline → 4-[6-(6-Chloro-4-methyl-pyridin-3-ylamino)-5-methyl-pyrimidin-4-yloxy]-piperidine-1-carboxylic Acid Isopropyl Ester

https://huagongshe.com/reaction/1036779

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참여 물질

역할이름HCID투입량
반응물3-Amino-6-chloro-4-picolineHCID 2734425—
반응물4-(6-Chloro-5-methyl-pyrimidin-4-yloxy)-piperidine-1-carboxylic acid isopropyl esterHCID 11493357—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
촉매Biphenyl-3-yl-di-tert-butyl-phosphaneHCID 67201513—
용매1,4-DioxaneHCID 31275—
생성물4-[6-(6-Chloro-4-methyl-pyridin-3-ylamino)-5-methyl-pyrimidin-4-yloxy]-piperidine-1-carboxylic Acid Isopropyl EsterHCID 1146427429.1%

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온도120 °C

반응 단계

A mixture of 4-(6-chloro-5-methyl-pyrimidin-4-yloxy)-piperidine-1-carboxylic acid isopropyl ester (1.80 g, 5.74 mmol), palladium acetate (155 mg, 0.69 mmol), biphenyl-3-yl-di-tert-butyl-phosphane (21.5 mg, 0.072 mmol), sodium tert-butoxide (1.38 g, 14.4 mmol), and 6-chloro-4-methyl-pyridin-3-ylamine (838 mg, 5.80 mmol) in 20 mL dioxane was heated in microwave for 1 hour at 120° C. Solids were filtered off and mixture was purified by column chromatography (hexane/AcOEt) to give Compound A98 as a tanned solid (702 mg, 29%). 1H NMR (CDCl3, 400 MHz) δ 1.24-1.26 (d, 6H), 1.72-1.81 (m, 2H), 1.95-2.02 (m, 2H), 2.10 (s, 3H), 2.27 (s, 3H), 3.37-3.43 (m, 2H), 3.74-3.77 (m, 2H), 4.90-4.97 (m, 1H), 5.29-5.34 (m, 1H), 5.91 (s, 1H), 7.00 (s, 1H), 8.22 (s, 1H), 8.57 (s, 1H). Exact mass calculated for C20H26ClN5O3 419.17, found 420.4 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08546429B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-0727b16a84d64597bb1dd5b9c77dddfd
출처 메모uspto-grants-2013_10