HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylalanine amide → HCID 68921208, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylalanine amide | HCID 445694 | — |
| Reactant | 2-[2-(1-Carbamoylethylcarbamoyl)quinolin-6-yl]-1-cyclohexyl-1H-benzimidazole-5-carboxylic Acid | HCID 57603050 | — |
| Reactant | 2-[2-(1-Carbamoylethylcarbamoyl)quinolin-6-yl]-1-cyclohexyl-1H-benzimidazole-5-carboxylic Acid Ethyl Ester | HCID 68919557 | — |
| Product | HCID 68921208 | HCID 68921208 | — |
Reaction Steps
The title compound (5 mg yield) was prepared as described for Compound 497a using L-phenylalaninamide in place of L-alaninamide and hydrolyzed as described for Compound 497.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07511145B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-f65a74023abf49d7bf98eb90d732f5aa |
| Source note | uspto-grants-2009_03 |