HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonamide → HCID 178505163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | Methyl 3-[({2-[(diaminomethylidene)amino]-1,3-thiazol-4-yl}methyl)sulfanyl]propanimidate | HCID 12881442 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178505163 | HCID 178505163 | 92.1% |
Reaction Steps
In 10.2 ml of methanol were dissolved 1.27 g of methyl 3-[(2-guanidinothiazol-4-yl)methylthio]propionimidate and 0.86 g of methanesulfonamide and after reacting for 48 hours at room temperature, the solvent was distilled off under reduced pressure. Then, the residue formed was purified by a silica gel column chromatography using a mixture of chloroform and methanol (20:1→10:1) to provide 1.44 g amorphous N-methanesulfonyl-3-[(2-guanidinothiazol-4-yl)-methylthio]propionamidine. The product shows the following physicochemical properties:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04283408 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-346f90de3eff4283acb88e9e7f6c2cd3 |
| Source note | uspto-grants-1981_08 |