HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Isoleucine, ethyl ester → N-(12-Methoxy-1-oxododecyl)-L-isoleucine, Ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Isoleucine, ethyl ester | HCID 6602175 | — |
| Reactant | Ethylacetate heptane | HCID 21899848 | — |
| Product | N-(12-Methoxy-1-oxododecyl)-L-isoleucine, Ethyl ester | HCID 9929366 | — |
Reaction Steps
The title compound was prepared by the method of Example 14 using the title product of Example 44 (1.1 g, 4 mmol) instead of benzylamine. Chromatography of the crude residue on silica gel using 50--50 ethyl acetate-heptane as eluant gave the title compound (875 mg) as a white powder, m.p. 36.4-38.1° C. (DSC). The structure was supported by NMR, infrared spectroscopy, optical rotation ([α]36525 +81.9°, CHCl3), elemental analysis, and mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981580 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-da38cf06f6ba41fa94b9c5d75628cf7d |
| Source note | uspto-grants-1999_11 |