HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232023Generated: October 26, 2026
Sodium Hydroxide → 1-Methyl-3-amino-5-[3-(4-piperidinomethylpyrazol-1-yloxy)propylamino]-1,2,4-triazole
https://huagongshe.com/reaction/232023
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(4-Piperidinomethylpyrazol-1-yloxy)propylamine | HCID 13823214 | — |
| Reactant | methyl N-cyano-1-methyl-2-(phenylmethylene)-hydrazinecarboximidothioate | HCID 54323404 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-Methyl-3-amino-5-[3-(4-piperidinomethylpyrazol-1-yloxy)propylamino]-1,2,4-triazole | HCID 20030805 | — |
Reaction Steps
5 g of 3-(4-piperidinomethylpyrazol-1-yloxy)-propylamine and 4.9 g of methyl N-cyano-1-methyl-2-(phenylmethylene)-hydrazinecarboximidothioate are combined, and heated at 70° C. for 1 hour. Thereafter, the reaction mixture is taken up with 40 ml of 1N hydrochloric acid, stirred for 1 hour at room temperature, rendered alkaline with sodium hydroxide solution and extracted with methylene chloride. The residue which remains after the solvent has been expelled is chromatographed over neutral Al2O3 (activity level III), using methylene chloride/3% strength methanol as the mobile phase. The oily title compound is reacted with tartaric acid in isopropanol to give an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04851410 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-138c7c0278b04dafbb97a21f50060891 |
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| Source note | uspto-grants-1989_07 |
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