HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451283Generated: October 26, 2026
Methylamine → N-methyl-4-(pyridin-3-yl)but-3-yn-1-amine
https://huagongshe.com/reaction/1451283
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-(Pyridin-3-yl)but-3-yn-1-ol | HCID 10582917 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-methyl-4-(pyridin-3-yl)but-3-yn-1-amine | HCID 15860335 | 546.1% |
Reaction Steps
An aqueous methylamine solution (5mL, 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05604231 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-3ba37f9985b641cf8039337702e35d27 |
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| Source note | uspto-grants-1997_02 |
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