HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606040Generated: October 30, 2026
Triethylamine → N-[2-chloro-4-(prop-2-ynylamino)quinolin-3-yl]-2-ethoxyacetamide
https://huagongshe.com/reaction/606040
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethoxyacetyl chloride | HCID 84189 | — |
| Reactant | 2-chloro-N4-prop-2-ynylquinoline-3,4-diamine | HCID 86247581 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[2-chloro-4-(prop-2-ynylamino)quinolin-3-yl]-2-ethoxyacetamide | HCID 86247582 | 79% |
Reaction Steps
Ethoxyacetyl chloride (89%, 28 g, 0.20 mol) was added dropwise to a solution of 2-chloro-N4-prop-2-ynylquinoline-3,4-diamine (43.5 g, 0.188 mol) and triethylamine (39 mL, 0.28 mol) in dichloromethane (600 mL) at 6° C. After two hours, the reaction mixture was diluted with dichloromethane and washed with saturated aqueous sodium bicarbonate. The aqueous layer was back-extracted with dichloromethane three times. The organic layers were combined and washed twice with water and brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting brown solid was triturated with toluene with heating. A fine tan solid was isolated by filtration, rinsed with diethyl ether, and dried to yield N-[2-chloro-4-(prop-2-ynylamino)quinolin-3-yl]-2-ethoxyacetamide (47.2 g).
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-9460237b00024437a28352fe8d20981e |
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| Source note | uspto-grants-2011_03 |
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