HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]piperidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-[(Tert-butoxy)carbonyl]piperidine-2-carboxylic acid | HCID 581831 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 1,7-Diphenyl-4-aminoheptane hydrochloride | HCID 21892255 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]piperidine-1-carboxylic acid tert-butyl ester | HCID 12136765 | — |
Reaction Steps
1-(tert-Butoxycarbonyl)-piperidine-2-carboxylic acid (3.00 g; 13.1 mmol) is dissolved in methylene chloride (100 mL) at ambient temperature. 1,7-Diphenyl-4-aminoheptane hydrochloride (1) (4.77 g; 15.7 mmol), diisopropylethylamine (7.3 mL; 41.9 mmol), and PyBOP (8.17 g; 15.7 mmol) are added sequentially. The mixture is stirred for 15 hours at ambient temperature then concentrated in vacuo at 40° C. The residue is purified via silica gel chromatography with gradient elution (10%→30% ethyl acetate in hexanes) affording the desired product as an oil. ESMS: MH+ 479.4
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809093B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-11aa5b13d11a4930b4b017cacd4880f6 |
| Source note | uspto-grants-2004_10 |