HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 4-phthalimidobutyl ketone → 2-(2-Methylguanidino)-4-(4-phthalimidobutyl)thiazole hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 4-phthalimidobutyl ketone | HCID 14506404 | — |
| Reactant | (N-methylamidino)thiourea | HCID 178485127 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Methylguanidino)-4-(4-phthalimidobutyl)thiazole hydrobromide | HCID 20280162 | — |
Reaction Steps
To a solution of (N-methylamidino)thiourea (0.4 g.) in hot ethanol (20 ml.) was added N-(6-bromo-5-oxohexyl)phthalimide (1.5 g.). The mixture was heated under reflux for 1 hour, cooled and evaporated to dryness. The residue was triturated with acetonitrile and the resulting solid was filtered and dried to give 2-(2-methylguanidino)-4-(4-phthalimidobutyl)thiazole hydrobromide, m.p. 210°-212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04234735 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-f7afa53e42e3496f8b62ad8ae58b9534 |
| Source note | uspto-grants-1980_11 |