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HRID 66697作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/66697

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

95 parts of isopropylaminosulfonyl chloride were stirred into a mixture of 96 parts of N-carbomethoxy-O-isopropyl-isourea and 73 parts of triethylamine in 700 parts of tetrahydrofuran at 10°-15° C., in the course of 25 minutes. After having been stirred 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. 130 parts of N-carbomethoxy-N'-isopropylsulfamyl-O-isopropylisourea, of melting point 62°-64° C., were obtained. 33.7 parts of this product were cyclized with 17.6 parts of 50 percent strength by weight sodium hydroxide solution in 30 parts of water for 5 minutes at 55°-60° C. After extraction with ether, acidification, filtering, washing the residue with water and drying, 22 parts of 6-isopropyl-3-isopropoxy-6H-1,2,4,6-thiatriazin-5-one-1,1-dioxide, of melting point 164°-167° C., were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04343648
出典データセットuspto-grants-1982_08
ORD IDord-81cc9971f06d4584a6c1ac7d88ab98f2
出典メモuspto-grants-1982_08