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HRID 1982097作成日:2026年10月25日

Water → N-[(4-Methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-1,3-benzoxathiole-4-sulfonamide

https://huagongshe.com/reaction/1982097

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl (4-methoxy-6-methylpyrimidin-2-yl)carbamateHCID 13072161—
反応物TrimethylaluminumHCID 16682925—
反応物1,3-Benzoxathiole-4-sulfonamideHCID 20137752—
触媒Hydrochloric AcidHCID 313—
溶媒Acetic AcidHCID 176—
溶媒DichloromethaneHCID 6344—
生成物N-[(4-Methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-1,3-benzoxathiole-4-sulfonamideHCID 20137750—

反応手順

To a solution of 2.2 g 1,3-benzoxathiole-4-sulfonamide, prepared in Example 13, in 50 ml methylene chloride at ambient temperature under nitrogen is added 5.5 ml trimethylaluminum (2M in toluene). After stirring 15 minutes at ambient temperature, 2.0 g of methyl[4-methoxy-6-methylpyrimidin-2-yl]carbamate, prepared according to the procedure of Example 3, is added and the reaction mixture is heated at reflux for 16 hours. The reaction mixture is cooled to ambient temperature and 75 ml water, 10 ml glacial acetic acid, and 10 drops hydrochloric acid are sequentially added. The organic phase is separated, dried, and the solvent removed under reduced pressure to give an oil. Crystallization of the oil from n-butyl chloride/ether gives a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04595407
出典データセットuspto-grants-1986_06
ORD IDord-652dc0895c1c4e03a66922b3ec3defd7
出典メモuspto-grants-1986_06