HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → HCID 178485205, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | HCID 178504068 | HCID 178504068 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 178485205 | HCID 178485205 | — |
Reaction Steps
A solution of 2-guanidino-4-[3-(3-methylsulphonyl-2-methylisothioureido)cyclohexyl]thiazole (0.25 g.) in methanol/chloroform 50:50 v/v (15 ml.) was treated with 20 ml. of 33% w/v methylamine in ethanol and the mixture allowed to stand at room temperature overnight. Evaporation of the solvent gave a gum which was dissolved in methanol (1 ml.) and to this solution was added an excess of maleic acid in acetone. The resulting solution was diluted with ether until crystallisation occurred, giving 2-guanidino-4-[3-(2-methylsulphonyl-3-methylguanidino)cyclohexyl]-thiazole hydrogen maleate monohydrate, m.p. 184°-187° (decomp).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04342765 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-8c3dbb999cf845789388e00f453c7701 |
| Source note | uspto-grants-1982_08 |