HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9378Generated: October 26, 2026
Triethylamine → 1-(7-Bromo-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol
https://huagongshe.com/reaction/9378
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Propanol, 1-amino-2-methyl- | HCID 95102 | — |
| Reactant | 7-Bromo-4-chloro-3-nitroquinoline | HCID 21984361 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(7-Bromo-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol | HCID 21984436 | 78.5% |
Reaction Steps
Triethylamine (17.35 mL, 124 mmol) was added to a solution of 7-bromo-4-chloro-3-nitroquinoline (29.84 g, 104 mmol) in dichloromethane (253 mL), and the reaction was cooled to 0° C. 1-Amino-2-methylpropan-2-ol (10.17 g, 114 mmol) was added dropwise, and then the reaction was allowed to warm to ambient temperature and stirred overnight. A precipitate formed and was isolated by filtration and washed with water. The crude solid was recrystallized from a mixture of isopropanol and acetonitrile to provide 27.78 g of 1-(7-bromo-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091214B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-264de42745e6441b818c0fd73a192dd5 |
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| Source note | uspto-grants-2006_08 |
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