HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamine → HCID 13137361, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamine | HCID 162203 | — |
| Reactant | HCID 13137348 | HCID 13137348 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13137361 | HCID 13137361 | — |
Reaction Steps
A mixture of 2-(5-dimethylaminomethyl-2-furanylmethylthio)ethylamine (1.71 g) and 2-nitroamino-5-(4-dimethylamino methylbenzyl)-4-pyrimidone (1.97 g) in ethanol (12 ml) was heated under reflux for 42 hr. The ethanol was evaporated at reduced pressure yielding 2-[2-(5-dimethylaminomethyl-2-furanylmethylthio)ethylamino]-5-(4-dimethylaminomethylbenzyl) 4-pyrimidone as a brown oily residue which was washed with hot water, cooled and mixed with dilute ethanolic hydrochloride acid. Excess of ethanol was evaporated under reduced pressure and the residue was recrystallised from isopropanol/methanol and from ethanol to give the trihydrochloride (1.85 g) as an off-white solid m.p. 180°-184° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04388317 |
| Source dataset | uspto-grants-1983_06 |
| ORD ID | ord-a27b488ecae645f9b822662ec7bfcc6a |
| Source note | uspto-grants-1983_06 |