HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281002Generated: October 30, 2026
Methyl iodide → Methyl 5-bromoquinoline-8-carboxylate
https://huagongshe.com/reaction/2281002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromoquinoline-8-carboxylic acid | HCID 59292860 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-bromoquinoline-8-carboxylate | HCID 71607288 | 14.5% |
Reaction Steps
To a solution of 5-Bromoquinoline-8-carboxylic acid (30 g, 0.119 mol, crude) in DMF (400 ml) was added potassium carbonate (41.12 g, 0.297 mol) and MeI (22.3 ml, 0.357 mol) at RT. The reaction mixture was stirred at RT for 12 h and the reaction completion was confirmed by TLC. After completion of reaction the reaction mixture was filtered and evaporated. The reaction mixture was basified with 10% NaHCO3 and extracted with ethyl acetate. The organic layer was washed with water, brine and dried over sodium sulphate and concentrated to afford the title compound as brown liquid (4.6 g). LCMS: Mass found (M+, 268). 1H NMR (DMSO-d6 400 MHz): δ 9.04-9.02 (dd, J=3.92, 5.68, Hz, 1H), 8.58-8.56 (m, 1H), 8.05-8.03 (d, J=7.72 Hz, 1H), 7.87-7.86 (d, J=7.76 Hz, 1H), 7.78-7.75 (dd, J=8.6, 12.8 Hz, 1H), 3.91 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139568B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-7b3c245f13774157925e73d63e9fa9e5 |
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| Source note | uspto-grants-2015_09 |
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