Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Ethyl 4-(3-bromopropyl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate | HCID 67539218 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70873332 | HCID 70873332 | — |
Reaction Steps
Piperidine (0.13 mL, 0.00132 mol) is added to a solution of 4-(3-bromopropyl)piperidine-1,4-dicarboxylic acid-1-tert-butyl ester-4-ethyl ester (0.1 gm, 0.00026 mol) in tetrahydrofuran (5 mL). The reaction mixture is heated at 60-65° C. for 3 hours. It is then cooled to room temperature, treated with demineralized water (12 mL) and extracted with ethyl acetate (2×20 mL). Combined extract is dried over sodium sulphate and concentrated under reduced pressure to get a crude residue which is purified by column chromatography (silica gel 230-400 mesh, methanol:dichloromethane, 1:9) to yield 4-(3-piperidin-1-yl propyl)piperidine-1,4-dicarboxylic acid-1-tert-butyl ester-4-ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266867B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-a9270880f4354a36980ba98f5de72aec |
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| Source note | uspto-grants-2016_02 |
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