HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520755Generated: October 25, 2026
Dichloromethane → N-[1-((6-chloropyridin-3-yl)methyl)pyridin-2(2H)-ylidene]acetamide
https://huagongshe.com/reaction/520755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-imine hydrochloride | HCID 86686930 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[1-((6-chloropyridin-3-yl)methyl)pyridin-2(2H)-ylidene]acetamide | HCID 86686933 | 17% |
Reaction Steps
Anhydrous dichloromethane (20 mL) was added to 118 mg (0.46 mmol) of 1-[(6-chloropyridin-3-yl)methyl]pyridine-2(1H)-imine hydrochloride obtained by the alternative method described in Synthesis Example 14, following which 159 μL (1.16 mmol, 116 mg) of triethylamine and 33 μL of acetyl chloride were added and the mixture was stirred at room temperature for 15 minutes. The reaction was stopped by adding water to the reaction mixture, and liquid-liquid extraction was carried out with chloroform and water. The organic phase was washed with a saturated aqueous solution of ammonium chloride, then concentrated. With the addition of hexane thereto, a solid settled out. The solid was collected by filtration and washed, then thoroughly dried, giving 21 mg of the target compound (yield, 17%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328068B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-29b9c9dc6ba248059537fa55dcf7de68 |
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| Source note | uspto-grants-2016_05 |
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