HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 478679, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ethyl 1,4-dihydro-4-oxo-7-(4-pyridyl)quinoline-3-carboxylate | HCID 3016145 | — |
| Reactant | HCID 10267135 | HCID 10267135 | — |
| Product | HCID 478679 | HCID 478679 | — |
Reaction Steps
The starting acid, 1,4-dihydro-4-oxo-1-(2-propenyl)-7-(4-pyridinyl)-3-quinolinecarboxylic acid (golden crystals, m.p. 259.5°-261° C. from methanol), was prepared by hydrolysis of the corresponding ethyl ester (yellow powder, m.p. 155°-157° C.), in turn prepared by alkylation of ethyl 1,4-dihydro-4-oxo-7-(4-pyridinyl)-3-quinolinecarboxylate with allyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959363 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-85be1de47ed144d08ea58814dad1209f |
| Source note | uspto-grants-1990_09 |