HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600477Generated: October 30, 2026
1-(2-Pyridyl)piperazine → HCID 22065963, compound
https://huagongshe.com/reaction/1600477
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(2-Pyridyl)piperazine | HCID 94459 | — |
| Reactant | 3-(Dimethylaminomethyl)-7-azaindole | HCID 5383549 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22065963 | HCID 22065963 | 96.9% |
Reaction Steps
To a solution of 3-(N,N-dimethylaminomethyl)-1H-pyrrolo[2,3-b]pyridine (258 mg, 1.39 mmol) (prepared in Example 1(a)) in toluene (10 mL) was added 1-(pyridin-2-yl)piperazine (233 mL, 250 mg, 1.53 mmol). The mixture was heated at reflux over night. Heating was discontinued and when the reaction temperature had reached room temperature the solid was filtered off and dried in vacuo to give 3-[4-(pyridin-2-yl)-piperazin-1-yl]methyl-1H-pyrrolo[2,3-b]pyridine as a colourless solid (395 mg, 93%). δH (300 MHz, CDCl3) 2.50 (4H, m, piperazinyl), 3.46 (4H, m, piperazinyl), 3.68 (2H, s), 6.61 (1H, dd, J=5.1 and 6.9), 6.78 (1H, d, J=8.6), 7.06 (1H, dd, J=4.7 and 7.8), 7.39 (1H, s), 7.51 (1H, dd, 6.9 and 8.6), 8.10 (1H, d, J=8.1), 8.12(1H, d, J=7.8), 8.22(1H, d, J=4.6),11.49(1H, br s); ESMS 294 (MH+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05976497 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-3e97126b04ab4424830813af8d3a8e2d |
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| Source note | uspto-grants-1999_11 |
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