戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1447155作成日:2026年10月27日

Triethylamine → N-carbomethoxy-N'-isopropylsulfamyl-O-isopropyl-isourea

https://huagongshe.com/reaction/1447155

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Isopropylsulphamoyl chlorideHCID 117737—
反応物methyl N-(C-propan-2-yloxycarbonimidoyl)carbamateHCID 140335035—
溶媒TetrahydrofuranHCID 8028—
生成物N-carbomethoxy-N'-isopropylsulfamyl-O-isopropyl-isoureaHCID 73682570—

反応条件

温度25 °C

反応手順

In the course of 25 minutes, 95 parts of isopropylaminosulfonyl chloride were stirred into a mixture of 96 parts of N-carbomethoxy-O-isopropylisourea and 73 parts of triethylamine in 700 parts of tetrahydrofuran at 10°-15° C. After then stirring for one hour at 25° C., the reaction mixture was extracted once with water and once with 0.5 N hydrochloric acid, dried and evaporated down under reduced pressure. This gave 130 parts of N-carbomethoxy-N'-isopropylsulfamyl-O-isopropyl-isourea, of melting point 62°-64° C. 33.7 parts of this product were cyclized with 17.6 parts of 50% strength by weight sodium hydroxide solution in 30 parts of water for 5 minutes at 55°-60° C. The mixture was extracted with ether and then acidified, and the product was filtered off, washed with water and dried, giving 22 parts of 6-isopropyl-3-isopropoxy-6H-1,2,4,6-thiatriazin-5-one,1,1-dioxide of melting point 164°-167° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04316015
出典データセットuspto-grants-1982_02
ORD IDord-96fd36b20f3d4ea093fbbaa376911c52
出典メモuspto-grants-1982_02