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HRID 131561作成日:2026年10月26日

6-Chloro-3-methyl-1-propyl-2,4(1H,3H)-pyrimidinedione → 6-Mercapto-3-methyl-1-propyl-pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/131561

反応式

関与物質

役割名称HCID仕込み量
反応物6-Chloro-3-methyl-1-propyl-2,4(1H,3H)-pyrimidinedioneHCID 816933—
反応物Sodium hydrosulfide hydrateHCID 16211346—
溶媒EthanolHCID 702—
生成物6-Mercapto-3-methyl-1-propyl-pyrimidine-2,4(1H,3H)-dioneHCID 86622710—

反応手順

A mixture of 6-chloro-3-methyl-1-propyl-pyrimidine-2,4(1H,3H)-dione (3.76 g), sodium hydrosulphide hydrate (6 g) and ethanol (100 ml) was stirred at room temperature for 48 hours then concentrated in vacuo. The residue was dissolved in water (500 ml) and washed with ethyl acetate (2×100 ml). The aqueous phase was acidified with dilute hydrochloric acid, then extracted with ethyl acetate (3×100 ml). The combined organic phase was dried (MgSO4) and evaporated to leave a pale yellow solid which was used directly in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384950B2
出典データセットuspto-grants-2008_06
ORD IDord-aa2686d9fed644a8b4ea57c0b60b8015
出典メモuspto-grants-2008_06