HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-[4-(1-Piperidinylmethyl)phenoxy]-1-propanamine → 1-Methyl-3-(methylthio)methyl-N-[3-[4-(1-piperidinylmethyl)phenoxy]propyl]-1H-1,2,4-triazole-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-[4-(1-Piperidinylmethyl)phenoxy]-1-propanamine | HCID 14086553 | — |
| Reactant | Methyl N-[2-(methylthio)acetyl]-1-methyl-2-(phenylmethylene)hydrazine carboximidothioate | HCID 53810570 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Methyl-3-(methylthio)methyl-N-[3-[4-(1-piperidinylmethyl)phenoxy]propyl]-1H-1,2,4-triazole-5-amine | HCID 20199162 | 73.7% |
Reaction Steps
Methyl N-[2-(methylthio)acetyl]-1-methyl-2-(phenylmethylene)hydrazine carboximidothioate (1.2 g) and 3-[4-(1-piperidinylmethyl)phenoxy]propanamine (0.9 g) were heated at 55° under water vacuum for 2 h. Additional carboximidothioate (0.09 g) was then added and the mixture heated for a further 1 h. The reaction mixture was dissolved in toluene (5 ml) and 5N hydrochloric acid (4 ml), stirred at room temperature for 18 h and the phases separated. The aqueous phase was basified to pH 10 with sodium carbonate and extracted with ethyl acetate to give an oil, which was chromatographed using ethyl acetate-methanol (3:1) to give the title compound (1.04 g) as an orange brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670448 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-b265223291b749da8093131a9ecb42b6 |
| Source note | uspto-grants-1987_06 |