HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703857Generated: October 26, 2026
Ammonia → 1-(Pyrid-2-oyl)-3-[1-(naphth-2-ylmethyl)piperid-4-yl]urea
https://huagongshe.com/reaction/703857
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethyl 2-pyridinecarboxylate | HCID 17307 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | [1-(Naphth-2-ylmethyl)piperid-4-yl]urea | HCID 13145794 | — |
| Product | 1-(Pyrid-2-oyl)-3-[1-(naphth-2-ylmethyl)piperid-4-yl]urea | HCID 19762398 | 32.5% |
Reaction Steps
Sodium (0.1 g, 4.35 mmol) in liquid ammonia (100-150 cm3) was stirred until the blue colour was discharged. A bomb was charged with [1-(naphth-2-ylmethyl)piperid-4-yl]urea (0.83 g, 2.93 mmol) and the liquid ammonia solution was added. The mixture was stirred at room temperature for 2 days then the bomb was cooled to -78° C., and ethyl picolinate (0.6 g, 3.97 mmol) was added. Stirring was continued for 3 hours at room temperature then the ammonia was allowed to evaporate and the gummy residue triturated with water then ethyl acetate. The ethyl acetate suspension was filtered to give recovered [1-(naphth-2-ylmethyl)piperid-4-yl]urea (0.33 g). The filtrate was evaporated and the residue chromatographed on silica eluting with chloroform then chloroform: ethyl acetate 4:1 to give the title compound (0.37 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04985438 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-3271ae2249a5462e89a0be5734811d49 |
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| Source note | uspto-grants-1991_01 |
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