HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9426Generated: October 29, 2026
Water → (7-Bromo-3-nitroquinolin-4-yl)-(5-chloropentyl)amine
https://huagongshe.com/reaction/9426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21984273 | HCID 21984273 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (7-Bromo-3-nitroquinolin-4-yl)-(5-chloropentyl)amine | HCID 21984402 | — |
Reaction Steps
A suspension of 5-(7-bromo-3-nitroquinolin-4-ylamino)pentan-1-ol (0.92 g, 2.6 mmol) in dichloromethane (13 mL) was cooled to 0° C.; thionyl chloride was added dropwise. The reaction was stirred for five minutes at 0° C. then allowed to warm to ambient temperature and stirred overnight. Saturated aqueous sodium bicarbonate (25 mL) was slowly added followed by water (25 mL). The aqueous layer was separated and extracted with dichloromethane (3×50 mL), and the combined organic fractions were dried over magnesium sulfate and concentrated under reduced pressure to provide 0.91 g of (7-bromo-3-nitroquinolin-4-yl)-(5-chloropentyl)amine as a yellow semisolid.
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-45a57d7b811b4b1789a26203d86721d9 |
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| Source note | uspto-grants-2006_08 |
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