HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-(6-Bromo-imidazo[1,2-a]pyrazin-8-ylamino)-benzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(6-Bromo-imidazo[1,2-a]pyrazin-8-ylamino)-benzoic acid ethyl ester | HCID 59754733 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(6-Bromo-imidazo[1,2-a]pyrazin-8-ylamino)-benzoic Acid | HCID 59754690 | 86.7% |
Reaction Steps
4-(6-Bromo-imidazo[1,2-a]pyrazin-8-ylamino)-benzoic acid ethyl ester (10.0 g; 27.7 mmol) is dissolved in 200 mL ethanol (200 proof) and 100 mL 1 N NaOH is added. The reaction is refluxed for 2 hours and then cooled to rt. The resulting solid is filtered and collected, then slurried up in 0.1 N HCl (75 mL) and extracted with CH2Cl2 (2×75 mL). The pooled CH2Cl2 layers is washed with brine, then dried over anhydrous sodium sulfate and concentrated in vacuo to provide 4-(6-bromo-imidazo[1,2-a]pyrazin-8-ylamino)-benzoic acid as a white solid (8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947835B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-e28e02d421b04cb7bf7e97ce092c7db0 |
| Source note | uspto-grants-2011_05 |