참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Isopropylsulphamoyl chloride | HCID 117737 | — |
| 반응물 | methyl N-(C-propan-2-yloxycarbonimidoyl)carbamate | HCID 140335035 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-carbomethoxy-N'-isopropylsulfamyl-O-isopropyl-isourea | HCID 73682570 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04316014 |
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| 출처 데이터셋 | uspto-grants-1982_02 |
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| ORD ID | ord-e298007e4b2445ebbde4aacd382923e1 |
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| 출처 메모 | uspto-grants-1982_02 |
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