HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178512719, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178478691 | HCID 178478691 | — |
| Reactant | HCID 178512727 | HCID 178512727 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178512719 | HCID 178512719 | — |
Reaction Steps
A mixture of 1-benzoyl-3-[2-(2-guanidinothiazol-4-ylmethylthio)ethyl]thiourea (0.394 g), histamine dihydrochloride (0.276 g), triethylamine (0.20 g), silver nitrate (0.204 g) and dimethyl formamide (20 ml) was stirred at room temperature overnight. After filtration the solution was evaporated to dryness and the residue purified by preparative thin layer chromatography (Merck 60F-254 plates developed with ethyl acetate/ethanol/ammonia (s.g. 0.88) 6:1:1 v/v/v). Isolation of the main band (RF 0.3) gave an oil which crystallized on trituration with acetone to give 1-benzoyl-2-[2-(2-guanidinothiazol-4-ylmethylthio)ethyl]-3-[2-(imidazol-4-yl)ethyl]guanidine, decomposing at 147°-150° after softening at 115°-117°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04309435 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-eb7c5fa09e5d4b948d513a19dfe4453f |
| Source note | uspto-grants-1982_01 |