HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → N-tert-Butoxycarbonyl-3-(3-pyridyl)alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | Boc-3-(3-pyridyl)-Ala-OH | HCID 7020919 | — |
| Reactant | 1,7-Diphenyl-4-aminoheptane hydrochloride | HCID 21892255 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-tert-Butoxycarbonyl-3-(3-pyridyl)alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide | HCID 59885582 | — |
Reaction Steps
N-tert-Butoxycarbonyl-3-(3-pyridyl)-alanine (1.00 g; 3.76 mmol) is dissolved in methylene chloride (25 mL) at ambient temperature. 1,7-Diphenyl-4-aminoheptane hydrochloride (1) (1.37 g; 4.51 mmol), N,N-diisopropylethylamine (1.55 g; 12.0 mmol) and PyBOP (2.34 g; 4.51 mmol) are added sequentially. The reaction is stirred for 2.5 hours at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography (60%→80% ethyl acetate in hexanes) affording the desired product (84) as a solid. ESMS:MH+ 516.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135483B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-a5cd2f13116a4023bcb3a61d6395d6d4 |
| Source note | uspto-grants-2006_11 |