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HRID 264803作成日:2026年10月26日

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

https://huagongshe.com/reaction/264803

反応式

関与物質

役割名称HCID仕込み量
反応物1-Methyl-3-pyrrolidinolHCID 93074—
反応物3-Butyloxy-4-methanesulfonyl-1,2,5-thiadiazoleHCID 19600307—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物3-Butoxy-4-(1-methyl-pyrrolidin-3-yloxy)-[1,2,5]thiadiazoleHCID 10825055—

反応手順

A solution of 1-methyl-3-pyrrolidinol (0.6 g, 0.0059 mol) in THF (20 mL) was treated with 1.6M 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646289
出典データセットuspto-grants-1997_07
ORD IDord-08d74c03007f48d48c00e453ab59cd9a
出典メモuspto-grants-1997_07