HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibenzylamine → HCID 59885610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 23718677 | HCID 23718677 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59885610 | HCID 59885610 | — |
Reaction Steps
Lithium (R)-1-[2-hydroxy-3-(quinolin-5-yloxy)-propyl]-piperidine-4-carboxylate (32) (100 mg; 0.297 mmol) is dissolved in methylene chloride (3 mL) at ambient temperature. Dibenzylamine (41) (62 mg; 0.312 mmol), N,N-diisopropylethylamine (85 mg; 0.654 mmol) and PyBOP (186 mg; 0.357 mmol) are added sequentially. The reaction is stirred for 18 hr. at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography with gradient elution (90% ethyl acetate in hexanes, then 50%→100% acetone in hexanes) affording the desired product (42) as a solid. CIMS (NH3CI): 510 (MH+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135483B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-590d6655ea164ce3ac0433fd3b3e4512 |
| Source note | uspto-grants-2006_11 |