HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606064Generated: October 30, 2026
Sodium Dithionite → Tert-butyl 2-[(3-amino-2-chloroquinolin-4-yl)amino]ethylcarbamate
https://huagongshe.com/reaction/606064
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Tert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamate | HCID 86616881 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl 2-[(3-amino-2-chloroquinolin-4-yl)amino]ethylcarbamate | HCID 86616882 | 62.9% |
Reaction Steps
A solution of Na2S2O4 (10.3 g, 50.4 mmol) in water (40 mL) was added to a solution of tert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamate (3.70 g, 10.1 mmol). A white solid precipitated immediately and after 30 min the precipitate was removed by filtration. The filtrate was concentrated under reduced pressure, was diluted with saturated aqueous sodium bicarbonate, and was extracted with dichloromethane three times. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered, and concentrated to a pale yellow oil. Purification by flash chromatography (silica gel, gradient elution with 2:1 to 1:1 hexanes/ethyl acetate) afforded tert-butyl 2-[(3-amino-2-chloroquinolin-4-yl)amino]ethylcarbamate (2.14 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915281B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-fe5cbc5da5ea4440bc6daf92dbb116ea |
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| Source note | uspto-grants-2011_03 |
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