HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → HCID 15581179, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 178499160 | HCID 178499160 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15581179 | HCID 15581179 | 46% |
Reaction Steps
To a mixture of 3.3 g (0.013 mol) of 3-carbomethoxy-4-hydroxy-7-methyl-pyrido[3',2':4,5]thieno[3,2-C]pyridazine, 3.8 g potassium bicarbonate, in 90 ml of anhydrous DMF was slowly added 9 ml of ethyl bromide and stirring was continued at 60°-70° C. for 3 hours. The solvent was then removed, the residue was diluted with water and filtered to give 3.4 g of crude product. Crystallization from EtoAc-hexane gave 1.8 g (46%) of pure 3-carbethoxy-4-ethoxy-7-methyl pyrido[3',2':4,5]thieno[3,2-C]pyridazine; m.p. 158°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04355164 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-c71c700273384af1a1f1314b5d69b239 |
| Source note | uspto-grants-1982_10 |