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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1447163생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1447163

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-isopropylisourea and 73 parts of triethylamine in 700 parts of tetrahydrofuran in the course of 25 minutes, at 10°-15° C. 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 concentrated under reduced pressure. This gave 130 parts of N-carbomethoxy-N'-isopropylsulfamyl-O-isopropylisourea, of melting point 62°-64° C. 33.7 parts of this product were cyclized by means of 17.6 parts of 50% strength by weight sodium hydroxide solution in 30 parts of water in the course of 5 minutes at from 55° to 60° C. Extraction with ether, acidification, washing with water and drying gave 22 parts of 6-isopropyl-3-isopropoxy-5,6-dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxide, of melting point 164°-167° C. This constitutes active ingredient No. 4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04316014
출처 데이터셋uspto-grants-1982_02
ORD IDord-e298007e4b2445ebbde4aacd382923e1
출처 메모uspto-grants-1982_02