HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 19390564, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Aminoquinoline-2-carboxylic acid | HCID 22503957 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19390564 | HCID 19390564 | — |
Reaction Steps
4-Amino-2-quinoline carboxylic acid (800 mg, 4.2 mmol) in DMF (10 ml) and K2CO3 (1.17 g, 8.5 mmol) was stirred at ambient temperature in the presence of allyl bromide (1.47 ml, 17 mmol) for 24 hours. The solvent was evaporated and the crude residue purified by subjecting to silico-gel chromatography, eluting with petroleum ether ethyl acetate 1/1) to give 2-allyloxycarbonyl-4-amino-quinoline (170 mg, NMR (CDCls): δ4.75-5 (m, 4H); 5.2-5.0 (m, 2H); 5.9-6.35 (m, 1H); 7.35-8.3 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441949 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-4cffe37e8603424c81bf6b93264f10b7 |
| Source note | uspto-grants-1995_08 |