HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanimidamide, N,N-diphenyl- → HCID 73681571, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanimidamide, N,N-diphenyl- | HCID 78296 | — |
| Reactant | 1-(2-Hydroxyethyl)-4-methylquinolin-1-ium bromide | HCID 12016691 | — |
| Reactant | HCID 70525732 | HCID 70525732 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 73681571 | HCID 73681571 | — |
Reaction Steps
On an oil bath, 2.7 g of 1-(2-hydroxyethyl)-4-methylquinolinium bromide and diphenylformamidine were heated for 5 minutes to melt them. Thereto was added 150 ml of ethanol, and the resulting mixture was boiled, upon which 1-(2-hydroxyethyl)-4-(2-anilinovinyl)-quinolinium bromide was crystallized. Then, 2.5 g of 1-hydroxyethyl-4-methylquinolinium bromide and 10 ml of triethylamine were added thereto and subjected to reaction under reflux for one hour. After completion of the reaction, the reaction product was cooled and the crude crystals thus obtained were recrystallized from methanol to obtain 2 g of the objective compound (melting point 262° C.) which was dark green. Its maximum absorption wavelength as measured in methanol was 707 nm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04386146 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-abc1f3a6e629414085d9452d80fcc2e9 |
| Source note | uspto-grants-1983_05 |