HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Nitro-S-methylisothiourea → HCID 178512642, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Nitro-S-methylisothiourea | HCID 135927615 | — |
| Reactant | HCID 178512644 | HCID 178512644 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178512642 | HCID 178512642 | — |
Reaction Steps
To a solution of 2-guanidino-4-(4-aminobutyl)thiazole (0.426 g.) in ethanol (10 ml.) was added 2-methyl-1-nitroisothiourea (0.270 g.). The mixture was heated under reflux for 4 hours, allowed to cool to room temperature, evaporated to dryness and the residue triturated with alcohol. The product was filtered off and dried to give 2-guanidino-4-[4-(2-nitroguanidino)butyl]thiazole, m.p. 180°-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04234735 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-0c3a8d7cf5e74b648bdb43fb26e20ba0 |
| Source note | uspto-grants-1980_11 |