HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Aspartic Acid → HCID 53241120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Aspartic Acid | HCID 5960 | — |
| Reactant | N-Benzylglycine ethyl ester | HCID 80908 | — |
| Reactant | D-Aspartic Acid | HCID 83887 | — |
| Reactant | methyl (2R)-2-(benzylamino)propanoate | HCID 10987118 | — |
| Product | HCID 53241120 | HCID 53241120 | — |
Reaction Steps
The title compound was prepared according to the procedure outlined in Example 255 substituting L-aspartic acid for D-aspartic acid and (R)-methyl 2-(benzylamino)propanoate for N-benzylglycine ethyl ester. Purification via flash chromatography (0-30% methanol/dichloromethane) afforded the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 6.84-7.01 (m, 3H), 6.73-6.85 (m, 1H), 4.35-4.51 (m, 1H), 3.99-4.14 (m, 1H), 2.80-3.28 (m, 6H), 1.95-2.14 (m, 1H), 1.66-1.85 (m, 1H), 1.20 (d, J=6.44 Hz, 3H); MS (DCI) m/z 219 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546377B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-6276ac8ee3d14d18a3f609d416f66510 |
| Source note | uspto-grants-2013_10 |