HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097597Generated: October 31, 2026
Triethylamine → Tert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamate
https://huagongshe.com/reaction/1097597
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | 2,4-Dichloro-3-nitroquinoline | HCID 2785138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamate | HCID 86616881 | 94.9% |
Reaction Steps
Triethylamine (30.98 g, 306.1 mmol) was added to a solution of 2,4-dichloro-3-nitroquinoline (50.0 g, 204 mmol) in DMF (200 mL). A solution of N-Boc-ethylenediamine (32.7 g, 204 mmol) in DMF (100 mL) was then added in small portions. The reaction was stirred at room temperature, and then most of the DMF was removed under reduced pressure. Water (600 mL) was added to the residue, and the mixture was stirred for three hours. A solid formed and was isolated by filtration, washed with water, and dried under house vacuum to provide 71 g of tert-butyl 2-[(2-chloro-3-nitroquinolin-4-yl)amino]ethylcarbamate as a yellow solid. A portion of the material (15 g) was dissolved in dichloromethane (200 mL), and the resulting solution was washed with brine (2×100 mL) and deionized water (2×100 mL), dried over magnesium sulfate, filtered, concentrated under reduced pressure, and further dried on a vacuum pump for three days to provide 13.99 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143270B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-80caf528aa55472f8e1bfb82de3a059b |
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| Source note | uspto-grants-2012_03 |
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