HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glutaric anhydride → HCID 22040206, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glutaric anhydride | HCID 7940 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86583531 | HCID 86583531 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22040206 | HCID 22040206 | — |
Reaction Steps
In analogy to Example 70.4–6, from the methyl (RS)-(3-amino-4-methoxy-phenyl)-(4-cyano-phenylamino)-acetate described in Example 70.3, glutaric anhydride and Hünig's base in DMF there was obtained (RS)-4-{5-[(4-cyano-phenylamino)-methoxycarbonyl-methyl]-2-methoxy-phenylcarbamoyl}-butyric acid, which was subsequently converted via (RS)-4-{5-[carboxy-(4-cyano-phenylamino)-methyl]-2-methoxy-phenylcarbamoyl}-butyric acid into (RS)-(E)- and/or -(Z)-4-(5-{carboxy-[4-(N-hydroxycarbamimidoyl)-phenylamino]-methyl}-2-methoxy-phenylcarbamoyl)-butyric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071212B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-2063ef9bf60b47c195f8389bf096c4d4 |
| Source note | uspto-grants-2006_07 |