HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166700Generated: October 31, 2026
5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamine → HCID 13137363, compound
https://huagongshe.com/reaction/2166700
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamine | HCID 162203 | — |
| Reactant | HCID 13137346 | HCID 13137346 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13137363 | HCID 13137363 | — |
Reaction Steps
A solution of 2-(5-dimethylaminomethyl-2-furanylmethylthio)ethylamine (1.29 g) and 2-nitroamino-5-(5-dimethylaminomethyl-2-furanylmethyl)-4-pyrimidone in pyridine (15 ml) was heated under reflux for about 20 hr. The pyridine was evaporated at reduced pressure. The last traces of pyridine were removed by azeotroping with water and water removed by azeotroping with n-propanol. The oily residue was chromatographed on a silica gel column eluting with methanol in ethyl acetate (10% v/v). Evaporation of the eluant yielded 2-[2-(5-dimethylaminomethyl-2-furanylmethylthio)ethylamino]-5-(5-dimethylaminomethyl-2-furanylmethyl)-4-pyrimidone as an oil which was converted to its trihydrochloride using an excess of ethanolic HCl. The salt was recrystallised from isopropanol yielding a white solid (0.72 g) m.p. 181°-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04388317 |
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| Source dataset | uspto-grants-1983_06 |
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| ORD ID | ord-8329ebea82264fdfbd8e69120e63b925 |
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| Source note | uspto-grants-1983_06 |
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