HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 86754978, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178468388 | HCID 178468388 | — |
| Reactant | HCID 178478806 | HCID 178478806 | — |
| Reactant | HCID 178512721 | HCID 178512721 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86754978 | HCID 86754978 | — |
Reaction Steps
A process for preparing Form A of N-[[[2-[[[2-[(diaminomethylene)amino]-4-thiazolyl]methyl]thio]ethyl]amino]methylene]-4-bromo-benzenesulfonamide of claim 1 which comprises reacting [4-[[(2-aminoethyl)thio]methyl]-2-thiazolyl]guanidine dihydrochloride with ethyl 4-bromo-benzene-sulfonylformimidate formimidate in methanol and in the presence of potassium hydroxide, followed by filtering and adding isopropanol over the filtrate to obtain N-[[[2-[[[2-(diaminomethylene)amino]-4-thiazolyl]methyl]thio]ethyl]amino]methylene]-4-bromo-benzenesulfonamide isopropanolate dissolving in methanol, filtering, and adding to water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06005115 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-ee9eab03a4e24b6692cdca3a8ddb2891 |
| Source note | uspto-grants-1999_12 |