HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351514Generated: October 26, 2026
3,4-Dibromopyridine → HCID 10111818, compound
https://huagongshe.com/reaction/1351514
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dibromopyridine | HCID 817106 | — |
| Reactant | 4-Aminomethyl-1-N-Cbz-piperidine | HCID 21955499 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 10111818 | HCID 10111818 | — |
Reaction Steps
A mixture of benzyl-4-(aminomethyl)piperidine-1-carboxylate (EXAMPLE 13, Step 1, 0.20 g, 0.81 mmol), 3,4-dibromo-pyridine (Chem. Abstracts, 58:5627) (0.19 g, 0.81 mmol) in IPA (0.5 mL) was heated at 100° C. in a sealed reaction tube for 7 h, then concentrated in vacuo. The residue was purified by silica gel chromatography (DCM IPA hexane)) to give 4-[(3-Bromo-pyridin-4-ylamino)-methyl]-piperidine-1-carboxylic acid benzyl ester. M.S. (M+1): 405.27
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217716B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-178a1dc1d9294f59a6a6a7064c79b542 |
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| Source note | uspto-grants-2007_05 |
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