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HRID 2720생성일: 2026년 10월 24일

Methylamine → N-methyl-4-(pyridin-3-yl)but-3-yn-1-amine

https://huagongshe.com/ko/reaction/2720

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물4-(Pyridin-3-yl)but-3-yn-1-olHCID 10582917—
용매WaterHCID 962—
생성물N-methyl-4-(pyridin-3-yl)but-3-yn-1-amineHCID 15860335546.1%

반응 단계

An aqueous methylamine solution (5 mL, 40%, 58.7 mmole) was mixed with XII (200 mg, 0.08 mmole) and stirred for 3 hr. in a sealed tube at 45° C. After the reaction was complete, water (10 mL) was added to the cooled reaction mixture, and the reaction mixture was extracted with chloroform (10×5 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated. The residue obtained was chromatographed on a silica gel column using methanol:chloroform (1:9) and then with a chloroform: methanol mixture containing 1% triethylamine as eluent. About 70 mg of XIII was obtained as a slightly yellow syrup, which was distilled at 110°-112° C., 0.04 mm Hg. XIII was converted to its mono fumarate salt form, which exhibits a melting point of 103°-104° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731314
출처 데이터셋uspto-grants-1998_03
ORD IDord-09f79ec740dc49de8727d8657531ecd2
출처 메모uspto-grants-1998_03