HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486915Generated: October 31, 2026
Sodium Hydroxide → 6-Bromo-4-(oxan-4-ylamino)quinoline-3-carboxylic acid
https://huagongshe.com/reaction/1486915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 6-bromo-4-(oxan-4-ylamino)quinoline-3-carboxylate | HCID 118498649 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Bromo-4-(oxan-4-ylamino)quinoline-3-carboxylic acid | HCID 118498620 | 100.6% |
Reaction Steps
On a larger scale, ethyl 6-bromo-4-(oxan-4-ylamino)quinoline-3-carboxylate (1925 g, 5.08 mol) was charged to the vessel with EtOH (12.5 L). 2M NaOH (12.5 L, 25.03 mol) was then added with an exotherm from 22-35° C. over the 20 minute addition. The batch was heated to 70-80° C. for 17 h at which point HPLC indicated 98.3% product and <1% starting material. The batch was concentrated in vacuo to remove EtOH and returned to the vessel. A 2M HCl solution (13 L) was then added until pH 5-6 was obtained maintaining a batch temperature below 50° C. An exotherm from 20-32° C. was observed over the 40 minute addition. A precipitate formed which was slurried at 20-25° C. for 1.5 h before filtration, washing with water until pH neutral (3×7 L). The collected solid was dried under vacuum at 70° C. to give 1794 g of desired material. Analytical data was consistent with that obtained from previous batches.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09428503B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-5d835e1edd0742e980ff5ef913b25830 |
|---|
| Source note | uspto-grants-2016_08 |
|---|