Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
(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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | (3-((tert-Butoxycarbonyl)amino)pyridin-4-yl)boronic acid | HCID 15366412 | — |
| 반응물 | tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)ethylcarbamate | HCID 66958848 | — |
| 생성물 | tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c][1,7]naphthyridin-1-yl)ethylcarbamate | HCID 66959244 | 20.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07879849B2 |
| 출처 데이터셋 | uspto-grants-2011_02 |
| ORD ID | ord-ddbbc949e372414fa05c7ecb15bde2d8 |
| 출처 메모 | uspto-grants-2011_02 |