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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360587생성일: 2026년 10월 25일

(3-((tert-Butoxycarbonyl)amino)pyridin-4-yl)boronic acid → tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c][1,7]naphthyridin-1-yl)ethylcarbamate

https://huagongshe.com/reaction/1360587

반응식

참여 물질

역할이름HCID투입량
반응물(3-((tert-Butoxycarbonyl)amino)pyridin-4-yl)boronic acidHCID 15366412—
반응물tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)ethylcarbamateHCID 66958848—
생성물tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c][1,7]naphthyridin-1-yl)ethylcarbamateHCID 6695924420.4%

반응 단계

A modification of the method described in Example 610 was used to couple tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)ethylcarbamate (2.08 g, 5.82 mmol) (Example 51, Parts A through G) with 3-[(tert-butoxycarbonyl)amino]pyridin-4-ylboronic acid (2.77 g, 11.6 mmol). After the first purification by IFC, 0.44 g of tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c][1,7]naphthyridin-1-yl)ethylcarbamate was obtained as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879849B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-ddbbc949e372414fa05c7ecb15bde2d8
출처 메모uspto-grants-2011_02