HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthaldehyde → N-[2(S)-(t-Butoxycarbonylamino)-3(S)-methylpentyl]-N-(1-naphthylmethyl)glycine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthaldehyde | HCID 6195 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N-(2(S)-(t-butoxycarbonylamino)-3(S)-methylpentyl)glycine methyl ester | HCID 10755806 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N-[2(S)-(t-Butoxycarbonylamino)-3(S)-methylpentyl]-N-(1-naphthylmethyl)glycine methyl ester | HCID 10526565 | — |
Reaction Steps
N-[2(S)-(t-Butoxycarbonylamino)-3(S)-methylpentyl]glycine methyl ester (2.00 g, 6.97 mmol) was dissolved in 1,2-dichloroethane (56 ml) and 3A molecular sieves were added followed by 1-naphthaldehyde (1.89 ml, 13.9 mmol) and sodium triacetoxyborohydride (665 g, 31.4 mmol). The mixture was stirred at ambient temperature for 16 h, and filtered through glass fiber paper and concentrated. The residue was partitioned between EtOAc and sat. NaHCO3 (100 ml/25 ml). The aqueous layer was extracted with EtOAc (3×50 ml). The organic layers were combined, dried (Na2SO4), filtered, and Concentrated to give 5.0 g of crude product which was purified by chromatography (SiO2, 15-33% ethyl acetate/hexane) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05523456 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-39281dd44897474a9df24c3d16165f1a |
| Source note | uspto-grants-1996_06 |