HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 1-(1-Tert-butoxycarbonylpiperidine-4-carbonyl)-piperidine-2 carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid | HCID 392871 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine | HCID 12992460 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(1-Tert-butoxycarbonylpiperidine-4-carbonyl)-piperidine-2 carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide | HCID 18727503 | — |
Reaction Steps
Piperidine-2-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (74) (1.00 g; 2.64 mmol) is dissolved in methylene chloride (25 mL) at ambient temperature. 1-tert-Butoxycarbonyl-piperidine-4-carboxylic acid (0.73 g; 3.17 mmol), N,N-diisopropylethylamine (0.75 g; 5.81 mmol) and PyBOP (1.65 g; 3.17 mmol) are added sequentially. The reaction is stirred for 16 hours at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography (30%→50% ethyl acetate in hexanes) affording the desired product (75) as a solid. ESMS: MH+ 590.6
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376514B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-bcba7d5d386d4774bd79666d9a05142a |
| Source note | uspto-grants-2002_04 |