HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829174Generated: October 31, 2026
Ammonia → {(3S)-3-(3,4-Dichlorophenyl)-1-[6-(dimethylamino)-2-pyridinyl]-6-oxopiperidinyl}acetaldehyde Hydrochloride
https://huagongshe.com/reaction/1829174
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (5S)-5-(3,4-dichlorophenyl)-5-(1,3-dioxolan-2-ylmethyl)-2-piperidinone | HCID 10882069 | — |
| Reactant | 6-bromo-N,N-dimethylpyridin-2-amine | HCID 14006062 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | {(3S)-3-(3,4-Dichlorophenyl)-1-[6-(dimethylamino)-2-pyridinyl]-6-oxopiperidinyl}acetaldehyde Hydrochloride | HCID 86593350 | — |
Reaction Steps
Copper (I) iodide (6.4 g, 33.3 mmol), potassium carbonate (6.3 g, 45.4 mmol) and 6-bromo-2-(dimethylamino)pyridine (WO 9843971) (9 g, 45.4 mmol) were added consecutively to a solution of (5S)-5-(3,4-dichlorophenyl)-5-(1,3-dioxolan-2-ylmethyl)-2-piperidinone (WO 9807722) (10 g, 30.3 mmol), in 1-methyl-2-pyrrolidinone (50 ml), and the mixture was stirred at 140° C. for 4 hours. The cooled mixture was poured into 4N hydrochloric acid, then carefully basified using 10% aqueous ammonia. The aqueous mixture was extracted with ethyl acetate (3×200 ml), and the combined organic extracts were washed with brine, dried (MgSO4) and evaporated under reduced pressure to give an orange oil. The crude product was purified by column chromatography on silica gel using methanol:dichloromethane (5:95) as eluant, and repeated using ethyl acetate as eluant. The product was treated with 1N ethereal hydrochloric acid, and evaporated under reduced pressure to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07060836B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-21c838b827c04abdbed331dd02a294dc |
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| Source note | uspto-grants-2006_06 |
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