HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 69188199, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (R)-Methyl 2-amino-6-((tert-butoxycarbonyl)amino)hexanoate | HCID 13645075 | — |
| Reactant | (4-Fluoro-3,5-dimethylphenyl)boronic acid | HCID 17750045 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69188199 | HCID 69188199 | 80% |
Reaction Steps
To a suspension of (R)-2-Amino-6-tert-butoxycarbonylamino-hexanoic acid methyl ester (3.000 g, 10.108 mmol), 3,5-dimethyl-4-fluorophenylboronic acid (3.398 g, 20.216 mmol), Cu(OAc)2 (2.019 g, 11.119 mmol), and molecular sieves 4 Å (7.591 g) in 45 mL of dichloromethane, was added triethylamine (2.8 mL, 20.216 mmol). After stirring at room temperature under O2 (1 atm) for 87 h, the reaction mixture was filtered through a pad of Celite and washed with dichloromethane. The filtrate was concentrated under reduced pressure. The product was isolated by Flash column chromatography (silica gel column) eluting with 0-30% ethyl acetate/hexanes to give the title compound as colorless oil (3.084 g, 80% yield). LC-MS: tR=9.8 min; m/z 383 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242174B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-b5c9e6337f2d4036a402df2f9110bec7 |
| Source note | uspto-grants-2012_08 |