HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586723Generated: October 30, 2026
1-Pyrrolidineethanamine → HCID 22335171, compound
https://huagongshe.com/reaction/586723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Pyrrolidineethanamine | HCID 1344 | — |
| Reactant | 6-Benzyl-2-chloro-5,6,7,8-tetrahydro-1,6-naphthyridine | HCID 16228747 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22335171 | HCID 22335171 | — |
Reaction Steps
Copper (II) sulphate (70 mg) was added to a solution of 6-benzyl-2-chloro-5,6,7,8-tetrahydro-[1,6]naphthyridine (0.75 g, 2.9 mmol)(WO9830560 Example 33 b) in 2-pyrrolidin-1-yl-ethylamine (3 ml) and the mixture was heated in an autoclave to 150° C. for 24 hours. The reaction mixture was cooled to room temperature and was diluted with dichloromethane (50 ml). The solution was washed with 50% ammonium hydroxide solution (50 ml). The phases were separated and the aqueous phase was extracted with dichloromethane (2×50 ml). The combined organic solutions were dried over magnesium sulphate and evaporated under reduced pressure. The residue was purified by chromatography on silica gel using ammonium hydroxide and methanol in dichloromethane as eluant (gradient from 0.5:5:95 to 0.7:7:93) to give the title compound as a yellow oil (0.9 g). LRMS: m/z (ES+) 337 [MH+]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936619B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-0c65a7d9b8264da78ff64c7c21ddd4df |
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| Source note | uspto-grants-2005_08 |
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