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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232025Generated: November 1, 2026

3-(4-Piperidinomethylpyrazol-1-yloxy)propylamine → 4-Methylamino-3-[3-(4-piperidinomethylpyrazol-1-yloxy)propylamino]-1,2,5-thiadiazole 1-oxide

https://huagongshe.com/reaction/232025

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Piperidinomethylpyrazol-1-yloxy)propylamineHCID 13823214—
Reactant3-Methoxy-4-methylamino-1,2,5-thiadiazole 1-oxideHCID 20030784—
SolventMethanolHCID 887—
Product4-Methylamino-3-[3-(4-piperidinomethylpyrazol-1-yloxy)propylamino]-1,2,5-thiadiazole 1-oxideHCID 1596189074.1%

Reaction Steps

2.4 g of 4-methylamino-3-methoxy-1,2,5-thiadiazole 1-oxide and 3.5 g of 3-(4-piperidinomethylpyrazol-1-yloxy)propylamine are dissolved in 50 ml of methanol, and the solution is left to stand at room temperature for 12 hours. The solution is then evaporated down and the residue is chromatographed over neutral Al2O3 (activity level III), using methylene chloride/3% strength methanol as the mobile phase. 4 g of the title compound are obtained, the product being crystallized from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851410
Source datasetuspto-grants-1989_07
ORD IDord-48c9ad669529453197a5fc909ac47d69
Source noteuspto-grants-1989_07