HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9873Generated: October 24, 2026
4-Pyridinecarboxaldehyde → (+/-)-7-(4-Pyridylmethyleneamino)-1,2,3,5,6,7,8,8a-octahydroindolizine
https://huagongshe.com/en/reaction/9873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Octahydroindolizin-7-amine | HCID 21988494 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (+/-)-7-(4-Pyridylmethyleneamino)-1,2,3,5,6,7,8,8a-octahydroindolizine | HCID 21988493 | 100.7% |
Reaction Steps
(±)-7-Amino-1,2,3,5,6,7,8,8a-octahydroindolizine (4.91 g (35.0 mmol), prepared as described in 1)) was dissolved in toluene (95 ml). To the solution were added 4-formylpyridine (3.34 ml, 35.0 mmol) and anhydrous magnesium sulfate (3.75 g, 31.2 mmol), and the resulting mixture was stirred at 70° C. for 3 hours. At the end of this time, the reaction mixture was filtered to remove the catalyst and the filtrate was concentrated by evaporation under reduced pressure, to give the title compound (8.08 g) as a pale yellow oil (yield quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091352B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-48980c3bc29d442994e424cd77e71dc8 |
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| Source note | uspto-grants-2006_08 |
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