HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → HCID 178421836, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Isopropyl Isothiocyanate | HCID 75263 | — |
| Reactant | 2-Amino-4-chloro-5-methylbenzene-1-sulfonamide | HCID 13001548 | — |
| Reactant | HCID 21197836 | HCID 21197836 | — |
| Product | HCID 178421836 | HCID 178421836 | — |
Reaction Steps
Starting from 2-amino-4-chloro-5-methylbenzenesulfonamide and isopropyl isothiocyanate, and following a procedure analogous to the one described in Example 4a, N-(2-amino-4-chloro-5-methylbenzenesulfonyl)-N′-isopropylthiourea was prepared; m.p. 120-122° C. Subsequent ring closure with phosgene by a procedure analogous to the one described in Example 4b gave the title compound; 1H-NMR (d6-DMSO), δ (ppm): 10.3 (br, 1H, NH), 7.68 (1H, arom.), 7.29 (1H, arom), 7.2 (br, 1H, NH), 4.0-3.8 (m, 1H, CH), 2.37 (s, 3H, CH3), 1.20 (d, 6H, CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06242443B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-77abd410cc224425859b08fc98b5c546 |
| Source note | uspto-grants-2001_06 |