HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 69785992, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | BOC-D-alanine | HCID 637606 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 18475823 | HCID 18475823 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69785992 | HCID 69785992 | — |
Reaction Steps
To (R)-N-(tert-butoxycarbonyl)alanine (1.09 g, 5.78 mmol) in dry CH2Cl2 (4 mL) under argon were added PYBOP (3.01 g, 5.78 mmol), 7-[(2-methoxyethoxy)methoxy]-1-(methylamino)naphthalene, as described above in Step B, (302 mg, 1.16 mmol), and N,N-diisopropylethylamine (1.00 mL, 5.75 mmol). The reaction mixture was stirred for 48 hrs, then partitioned between CH2Cl2 (500 mL) and 10% aqueous citric acid (150 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography on silica, eluting with a gradient of hexane −10% to 60% EtOAc to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06410534B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-91222a94e94a4889bf5fc81647edb445 |
| Source note | uspto-grants-2002_06 |