HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1,4-dihydro-1-[4-[4-(4-methoxyphenyl)-1-piperazinyl]-phenyl]-4-propyl-5H-tetrazol-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | N,N-Bis(2-chloroethyl)-4-methoxybenzenamine | HCID 15064 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(4-aminophenyl)-1,4-dihydro-4-propyl-5H-tetrazol-5-one monohydrochloride | HCID 23048854 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,4-dihydro-1-[4-[4-(4-methoxyphenyl)-1-piperazinyl]-phenyl]-4-propyl-5H-tetrazol-5-one | HCID 15125487 | 39% |
Reaction Steps
A mixture of 25 parts of N,N-bis(2-chloroethyl)-4-methoxybenzenamine, 25.5 parts of 1-(4-aminophenyl)-1,4-dihydro-4-propyl-5H-tetrazol-5-one monohydrochloride, 2 parts of potassium iodide and 200 parts of cyclohexanol was stirred and refluxed for 5 hours using a water-separator. The reaction mixture was cooled and neutralized with a sodium hydrogen carbonate solution. The product was filtered off and crystallized from 1-butanol, yielding 15.5 parts (39%) of 1,4-dihydro-1-[4-[4-(4-methoxyphenyl)-1-piperazinyl]-phenyl]-4-propyl-5H-tetrazol-5-one; mp. 189.7 ° C. (int. 33).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04931444 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-42b8aece752e48ff905e522bbec02a29 |
| Source note | uspto-grants-1990_06 |