HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Ethyl 4-[2-[1-(6-fluoro-3-pyridazinyl)-4-piperidinyl]ethoxy]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,6-Difluoropyridazine | HCID 19748273 | — |
| Reactant | Ethyl 4-[2-(4-piperidinyl)ethoxy]benzoate butanedioate | HCID 23056112 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-[2-[1-(6-fluoro-3-pyridazinyl)-4-piperidinyl]ethoxy]benzoate | HCID 14989295 | 64.3% |
Reaction Steps
A mixture 1.2 parts of 2,6-difluoropyridazine, 4 parts of ethyl 4-[2-(4-piperidinyl)-ethoxy]benzoate butanedioate(1:1), 5.3 parts of sodium carbonate and 141 parts of N,N-dimethylformamide was stirred for 48 hours at 60° C. After cooling, the reaction mixture was poured into water. The precipitated product was filtered off, washed with water and dissolved in trichloromethane. The organic layer was dried, filtered and evaporated. The residue was crystallized from 2-propanol. The product was filtered off and dried, yielding 2.4 parts (64.3%) of ethyl 4-[2-[1-(6-fluoro-3-pyridazinyl)-4-piperidinyl]-ethoxy]benzoate; mp. 131.9° C. (comp. 73).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04992433 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-aba27ace058f47e68d84de4154a6232f |
| Source note | uspto-grants-1991_02 |