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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1271560생성일: 2026년 10월 27일

3-Ethynylpyridine → (6-Methyl-2-pyridin-3-ylethynyl-pyridin-3-yl)amine

https://huagongshe.com/reaction/1271560

반응식

참여 물질

역할이름HCID투입량
반응물3-EthynylpyridineHCID 186003—
반응물2-Bromo-6-methylpyridin-3-amineHCID 14418051—
촉매HCID 178418476HCID 178418476—
용매TriethylamineHCID 8471—
생성물(6-Methyl-2-pyridin-3-ylethynyl-pyridin-3-yl)amineHCID 1035303649%

반응 단계

Following the same procedure as described in Example 1, (2-bromo-6-methyl-pyridin-3-yl)amine (200 mg, 1.07 mmol) reacted with (PPh3)2PdCl2 (37 mg, 0.05 mmol), Cul (10 mg, 0.05 mmol) and 3-ethynyl-pyridine (110 mg, 1.07 mmol) in triethylamine (1.6 ml). The crude residue was purified by flash chromatography (DCM-DCM/MeOH 97:3) to yield 100 mg (0.48 mmol, 49%) of (6-methyl-2-pyridin-3-ylethynyl-pyridin-3-yl)amine as a yellow powder. The hydrochloride of (6-methyl-2-pyridin-3-ylethynyl-pyridin-3-yl)amine was prepared as described in Example 1 to yield after trituration with pentane 145 mg (100%) of the title hydrochloride as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07205411B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-7cb582cbc27a4bc793c3f5db30ec7735
출처 메모uspto-grants-2007_04