HuagongsheHuagongshe Chemistry Print Report · For research reference only
Octylamine → HCID 9881109, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Octylamine | HCID 8143 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2R)-1-[(tert-butoxy)carbonyl]piperidine-2-carboxylic acid | HCID 688618 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9881109 | HCID 9881109 | — |
Reaction Steps
(R)-(+)-1-(tert-Butoxycarbonyl)-2-piperidinecarboxylic acid (Aldrich Chemical Company, Milwaukee, Wis.) (1.00 g; 4.36 mmol) is dissolved in methylene chloride (20 mL) at ambient temperature. n-Octylamine (0.620 g; 4.80 mmol), N,N-diisopropylethylamine (1.24 g; 9.60 mmol) and PyBOP (2.50 g; 4.80 mmol) are added sequentially. The reaction is stirred for 25 hours at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography using a gradient elution (20%→40% ethyl acetate in hexanes) affording the desired product (22) as an oil. ISMS: MH+341.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07018642B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-cb625815ead3441b8c631b7ebaacaf6d |
| Source note | uspto-grants-2006_03 |