HuagongsheHuagongshe Chemistry Print Report · For research reference only
(-)-2-Aminobutyric acid → (2S)-2-[(5-bromo-2-nitrophenyl)amino]butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (-)-2-Aminobutyric acid | HCID 80283 | — |
| Reactant | 4-Bromo-2-fluoro-1-nitrobenzene | HCID 2783362 | — |
| Reactant | (R)-2-(4-fluoro-2-nitrophenylamino)-butyric acid | HCID 69223325 | — |
| Product | (2S)-2-[(5-bromo-2-nitrophenyl)amino]butanoic acid | HCID 69223544 | — |
Reaction Steps
4-Bromo-2-fluoronitrobenzene was treated with (S)-2-aminobutyric acid according to the procedure for the preparation of (R)-2-(4-fluoro-2-nitrophenylamino)-butyric acid (see Example 1) to yield (2S)-2-[(5-bromo-2-nitrophenyl)amino]butanoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351709B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-cb2d6b71ee1645b096f83602f5fb7818 |
| Source note | uspto-grants-2008_04 |