HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432749Generated: October 29, 2026
Ethoxyacetyl chloride → HCID 21936599, compound
https://huagongshe.com/reaction/432749
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethoxyacetyl chloride | HCID 84189 | — |
| Reactant | Tert-butyl 2-{2-[(3-aminoquinolin-4-yl)amino]ethoxy)ethylcarbamate | HCID 12106200 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 21936599 | HCID 21936599 | 71.6% |
Reaction Steps
A solution of tert-butyl 2-{2-[(3-aminoquinolin-4-yl)amino]ethoxy}ethylcarbamate (18.04 g, 52.1 mmol) in 180 mL of pyridine was treated with 50 mg of 4-dimethylaminopyridine and chilled in an ice water bath. 2-ethoxyacetyl chloride (6.44 g, 52.6 mmol) was added dropwise to the solution. The reaction was stirred at room temperature for 3 h. The reaction was then heated to reflux with stirring. After 18 h the reaction was cooled and then concentrated. The residue was partitioned between CHCl3 (150 mL) and water (150 mL) and the layers were separated. The aqueous portion was extracted with CHCl3 (3×50 mL). The combined organic portions were washed with brine, dried over Na2SO4, filtered and concentrated to yield 15.47 g of tert-butyl 2-{2-[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]ethoxy}ethylcarbamate as a sticky yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06664265B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-08bd5c5b99884440a0f3c5ea6ef10fe6 |
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| Source note | uspto-grants-2003_12 |
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