HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254252Generated: October 25, 2026
4-Methylmorpholine → 6-Chloro-nicotinic Acid N'-(2-ethoxy-acetyl)-hydrazide
https://huagongshe.com/reaction/254252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Ethoxyacetyl chloride | HCID 84189 | — |
| Reactant | 6-Chloropyridine-3-carbohydrazide | HCID 2800177 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-nicotinic Acid N'-(2-ethoxy-acetyl)-hydrazide | HCID 58997482 | 83% |
Reaction Steps
(2-Ethoxy)-acetyl chloride [(1.72 g, 13.99 mmol), Tett. Lett., 35, (39), 7269; 1994)] was added to an ice-cold solution of 6-chloronicotinic acid hydrazide (2 g, 11.66 mmol) and N-methylmorpholine (1.92 mL, 17.49 mmol) in dichloromethane (60 mL) and the mixture was stirred at room temperature for 18 hours. The mixture was then washed with citric acid, sodium hydrogen carbonate solution and brine and the solvent was evaporated under reduced pressure to yield some title product as a white solid, 880 mg. The combined aqueous washings were extracted with ethyl acetate (×2) and the combined organic solutions were dried over sodium sulfate and concentrated in vacuo to afford a further crop of title compound as a pale yellow solid, 1.6 g (total yield of 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875615B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-a98d691c4edc4a7ea0579b35d0db799e |
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| Source note | uspto-grants-2011_01 |
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