HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66697Generated: October 26, 2026
Triethylamine → N-carbomethoxy-N'-isopropylsulfamyl-O-isopropyl-isourea
https://huagongshe.com/reaction/66697
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isopropylsulphamoyl chloride | HCID 117737 | — |
| Reactant | methyl N-(C-propan-2-yloxycarbonimidoyl)carbamate | HCID 140335035 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-carbomethoxy-N'-isopropylsulfamyl-O-isopropyl-isourea | HCID 73682570 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04343648 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-81cc9971f06d4584a6c1ac7d88ab98f2 |
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| Source note | uspto-grants-1982_08 |
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