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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Chloro-4-pyridineboronic acid | HCID 3861877 | — |
| 반응물 | 5-Bromo-N4-(tetrahydro-pyran-4-yl)-pyrimidine-2,4-diamine | HCID 58299673 | — |
| 촉매 | HCID 178418476 | HCID 178418476 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 5-(3-Chloro-pyridin-4-yl)-N4-(tetrahydro-pyran-4-yl)-pyrimidine-2,4-diamine | HCID 58300021 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08841312B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-633972e782a343608819f24c9088577b |
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| 출처 메모 | uspto-grants-2014_09 |
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