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HRID 1769596作成日:2026年10月25日

3-(Chloromethyl)pyridine hydrochloride → 6-ethyl-4-(3-pyridylmethyl)-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxide

https://huagongshe.com/reaction/1769596

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
反応物Lithium hydrideHCID 62714—
反応物6-ethyl-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxideHCID 135795659—
溶媒DimethylformamideHCID 6228—
生成物6-ethyl-4-(3-pyridylmethyl)-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxideHCID 2009700720%

反応条件

温度60 °C

反応手順

0.48 g (60 mmol) of lithium hydride is added in portions to a solution of 5.0 g (25 mmol) of 6-ethyl-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxide in 250 ml of DMF. The mixture is heated at 60° C. for 15 minutes, then 4.9 g (30 mmol) of 3-picolyl chloride hydrochloride are added and the mixture is heated at 80° C. for 3 hours. It is then largely concentrated, the residue is taken up with ethyl acetate and the mixture is extracted with 10% strength hydrochloric acid. The aqueous extract is neutralised and extracted with ethyl acetate. Relatively readily volatile impurities are removed by distillation in vacuo at 100° C./0.5 mm Hg and the residue is chromatographed. 1.4 g (20%) of 6-ethyl-4-(3-pyridylmethyl)-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxide are obtained as a highly viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05382585
出典データセットuspto-grants-1995_01
ORD IDord-a1c5d655e4234b35a21616054a292e2a
出典メモuspto-grants-1995_01