HuagongsheHuagongshe Chemistry Print Report · For research reference only
Succinic anhydride → Diisopropylethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | HCID 22040206 | HCID 22040206 | — |
| Product | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 22038928 | HCID 22038928 | — |
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, succinic anhydride and Hünig's base there was obtained (RS)-N-{5-[(4-cyano-phenylamino)-methoxycarbonyl-methyl]-2-methoxy-phenyl}-succinamidic acid, which was subsequently converted via (RS)-N-{5-[carboxy-(4-cyano-phenylamino)-methyl]-2-methoxy-phenyl}-succinamidic acid into (RS)-(E)- and/or -(Z)-N-(5-{carboxy-[4-(N-hydroxycarbamimidoyl)-phenylamino]-methyl}-2-methoxy-phenyl)-succinamidic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06242644B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-dba7fd8a29504bdba651765c4d7b8d98 |
| Source note | uspto-grants-2001_06 |