HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827138Generated: October 31, 2026
2,3-Dichloropyridine → HCID 10291987, compound
https://huagongshe.com/reaction/1827138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloropyridine | HCID 16988 | — |
| Reactant | 4-Aminomethyl-1-N-Cbz-piperidine | HCID 21955499 | — |
| Product | HCID 10291987 | HCID 10291987 | — |
Reaction Steps
A mixture of benzyl 4-(aminomethyl)piperidine-1-carboxylate (EXAMPLE 13, Step 1) (1 g, 4.03 mmol) and 2,3-dichloropyridine (0.25 g) was heated to 100° C. for 12 h. The reaction mixture was cooled and partitioned between EtOAc and pH5.2 citrate buffer. The organic layer was washed with brine, dried over anhydrous sodium sulfate and the solvent evaporated to give a crude product. Purification by flash column chromatography (5–50% EtOAc hexane) afforded the title compound. M.S (M+1): 360.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053089B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-f709966b7e664053965df0793c12cca1 |
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| Source note | uspto-grants-2006_05 |
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