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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66697생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Isopropylsulphamoyl chlorideHCID 117737—
반응물methyl N-(C-propan-2-yloxycarbonimidoyl)carbamateHCID 140335035—
용매TetrahydrofuranHCID 8028—
생성물N-carbomethoxy-N'-isopropylsulfamyl-O-isopropyl-isoureaHCID 73682570—

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04343648
출처 데이터셋uspto-grants-1982_08
ORD IDord-81cc9971f06d4584a6c1ac7d88ab98f2
출처 메모uspto-grants-1982_08