HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9417Generated: October 26, 2026
Sodium Dithionite → 7-bromo-N4-(4-chlorobutyl)quinoline-3,4-diamine
https://huagongshe.com/reaction/9417
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | (7-Bromo-3-nitroquinolin-4-yl)-(4-chlorobutyl)amine | HCID 21984395 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-bromo-N4-(4-chlorobutyl)quinoline-3,4-diamine | HCID 68817929 | 98% |
Reaction Steps
A suspension of (7-bromo-3-nitroquinolin-4-yl)-(4-chlorobutyl)amine (8.05 g, 22.5 mmol) in methanol (250 mL) was cooled to 0° C.; a solution of sodium hydrosulfite (19.5 g, 112 mmol) in water (80 mL) was added dropwise over a period of 30 minutes. The reaction was stirred at ambient temperature for two hours and then concentrated under reduced pressure. The residue was partitioned between dichloromethane (300 mL) and aqueous sodium bicarbonate (150 mL of 50%). The aqueous layer was separated and extracted with dichloromethane (2×50 mL). The combined organic fractions were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 7.25 g of crude 7-bromo-N4-(4-chlorobutyl)quinoline-3,4-diamine as a light brown semi-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-440122c60b11499ca2604e0ffa81145b |
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| Source note | uspto-grants-2006_08 |
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