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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4292생성일: 2026년 10월 23일

2,3-Diaminopyridine → 2-Amino-3-(2-methylbenzylamino)pyridine

https://huagongshe.com/ko/reaction/4292

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DiaminopyridineHCID 9956—
반응물2-MethylbenzaldehydeHCID 10722—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium cyanoborohydrideHCID 5003444—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물2-Amino-3-(2-methylbenzylamino)pyridineHCID 1382589134.4%

반응 단계

Molecular Sieves (16 g) was added to a solution of 2,3-diaminopyridine (8 g), 2-methylbenzaldehyde (8.81 g), and acetic acid (4.2 ml) in methanol (160 ml) and the mixture was stirred for 96 hours at room temperature. Sodium cyanoborohydride (4.61 g) was added portionwise to the mixture with stirring under ice-cooling over a period of 20 minutes. After being stirred for 3 hours, the mixture was made alkaline with aqueous sodium bicarbonate solution and filtered by suction. The filtrate was evaporated in vacuo, and to the residue was added water and then extracted with methylene chloride. The extract was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The crystalline residue was recrystallized from a mixture of ethyl acetate and n-hexane to give 2-amino-3-(2-methylbenzylamino)pyridine (5.38 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04725601
출처 데이터셋uspto-grants-1988_02
ORD IDord-8afe18d01bb54bda9ec3d89b8bd7890e
출처 메모uspto-grants-1988_02