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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458883Generated: October 27, 2026

Hexane → (S)-3-Butyloxy-4-(1-methyl-2-pyrrolidinylmethoxy)-1,2,5-thiadiazole

https://huagongshe.com/reaction/1458883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant(2S)-1-Methyl-2-pyrrolidinemethanolHCID 643492—
Reactant3-Butyloxy-4-methanesulfonyl-1,2,5-thiadiazoleHCID 19600307—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(S)-3-Butyloxy-4-(1-methyl-2-pyrrolidinylmethoxy)-1,2,5-thiadiazoleHCID 54562067—

Reaction Steps

A solution of (S)-1-methyl-2-pyrrolidinemethanol (0.86, 0.0075 mol) in THF (20 mL) was treated with 1.6M n-butyllithium in hexane (4.7 mL, 0.0075 mol). To the solution was added 3-butyloxy-4-methanesulfonyl-1,2,5-thiadiazole (1.2 g, 0.005 mol) and the reaction heated to reflux for 6.5 h. The solvent was evaporated, the residue acidified with cold 1N HCl, and the mixture extracted with ether. The aqueous was made basic and extracted with EtOAc. The extracts were washed with water, dried, and the solvent evaporated to give a liquid. The HCl salt (0.72 g) crystallized from EtOAc, m.p. 115°-116° C. (Compound 31).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852037
Source datasetuspto-grants-1998_12
ORD IDord-20d94e093ce64082afb50692b0cd7018
Source noteuspto-grants-1998_12