Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399661Generated: October 26, 2026

1-Methyl-3-pyrrolidinol → 3-Butoxy-4-(1-methyl-pyrrolidin-3-yloxy)-[1,2,5]thiadiazole

https://huagongshe.com/reaction/399661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-3-pyrrolidinolHCID 93074—
Reactant3-Butyloxy-4-methanesulfonyl-1,2,5-thiadiazoleHCID 19600307—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-Butoxy-4-(1-methyl-pyrrolidin-3-yloxy)-[1,2,5]thiadiazoleHCID 10825055—

Reaction Steps

A solution of 1-methyl-3-pyrrolidinol (0.6 g, 0.0059 mol) in THF (20 mL) was treated with 1.6 M n-butyllithium in hexane (3.1 mL), 0.005 mol). To the solution was added 3-butyloxy-4-methanesulfonyl-1,2,5-thiadiazole (1.0 g, 0.0042 mol) and the reaction heated to reflux overnight. The solvent was evaporated, the residue acidified with cold 1N HCl, and the mixture extracted with ether. The aqueous fraction was made basic, extracted with EtOAc, and the extracts washed with water. The extracts were dried and the solvent evaporated to give a liquid. The HCl salt (0.7 g) crystallized from EtOAc, m.p. 157°-158° C. (Compound 28).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05821371
Source datasetuspto-grants-1998_10
ORD IDord-53ca0e18f85144909105cbf7bf1b7536
Source noteuspto-grants-1998_10