Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1668653생성일: 2026년 10월 26일
Potassium Carbonate → (1H-Indol-4-ylmethyl)-(6-pyridin-3-yl-2-pyridin-2-yl-pyrimidin-4-yl)-amine
https://huagongshe.com/reaction/1668653
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | (1H-indol-4-yl)methanamine | HCID 280302 | — |
| 반응물 | 4-Chloro-2-(pyridin-2-yl)-6-(pyridin-3-yl)pyrimidine | HCID 28309111 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | (1H-Indol-4-ylmethyl)-(6-pyridin-3-yl-2-pyridin-2-yl-pyrimidin-4-yl)-amine | HCID 23653548 | — |
반응 단계
A solution of 4-chloro-6-pyridin-3-yl-2-pyridin-2-yl-pyrimidine (Intermediate A) (1 eq, 0.2 g), C-(1H-indol-4-yl)-methylamine (1.1 eq, 0.12 g) and K2CO3 (3 eq, 0.308 g) in NMP (6 ml) is heated using microwave radiation at 120° C. for 1 hour. After cooling to room temperature, the mixture is partitioned between EtOAc/water and the organic portion is separated, washed with brine, dried (MgSO4) and concentrated in vacuo. The crude residue is purified by mass directed preparative HPLC eluting with acetonitrile in water—0.1% TFA and the appropriate fractions are combined and concentrated in vacuo. The resulting residue is loaded onto a SCX-2 cartridge eluting with MeOH followed by 2M NH3 in MeOH. The methanolic ammonia fractions are concentrated in vacuo and dried under vacuum to afford the title compound [M+H]+=379.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07989458B2 |
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| 출처 데이터셋 | uspto-grants-2011_08 |
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| ORD ID | ord-b28b5156c4cc45c390324699be3e2f60 |
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| 출처 메모 | uspto-grants-2011_08 |
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