HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646864Generated: October 31, 2026
HCID 14209234, compound → HCID 14209219, compound
https://huagongshe.com/reaction/1646864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 14209234 | HCID 14209234 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14209219 | HCID 14209219 | 23.3% |
Reaction Steps
A mixture of 8.0 g of 3-bromo-N-(2-hydroxyethyl)-4-quinolinamine and 4 g of potassium-tert-butoxide in 220 ml of dimethylformamide was heated at reflux for 3 hours. The reaction mixture was cooled to room temperature and diluted with 200 ml of water and the product was extracted with 4 portions of 50 ml of dichloromethane (DCM). The DCM solution was dried over sodium sulfate and concentrated. The oily residue was dissolved in 150 ml of ethanol. To this solution 5 ml of concentrated HCl was added, the HCl salt was separated by filtration and recrystallized from ethanol. This crystalline material was dissolved in 75 ml of water and the solution made alkaline (pH=8) with a sodium bicarbonate solution. The free base was filtered and dried in vacuo to yield 1.3 g of white solid, mp 175°-176° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05182275 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-74fa1593636042f2b1e78778f98cef3a |
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| Source note | uspto-grants-1993_01 |
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