HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-2-methylbenzoic acid → (2S)-2-[[1-cyclohexyl-2-(3-furyl)-6-methyl-benzimidazole-5-carbonyl]amino]-3-(5-hydroxy-1H-indol-3-yl)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-2-methylbenzoic acid | HCID 348269 | — |
| Reactant | HCID 23378470 | HCID 23378470 | — |
| Reactant | methyl (2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoate hydrochloride | HCID 24802218 | — |
| Product | (2S)-2-[[1-cyclohexyl-2-(3-furyl)-6-methyl-benzimidazole-5-carbonyl]amino]-3-(5-hydroxy-1H-indol-3-yl)propanoic acid | HCID 491059 | — |
| Product | HCID 3012619 | HCID 3012619 | — |
Reaction Steps
1-Cyclohexyl-2-furan-3-yl-6-methyl-1H-benzimidazole-5-carboxylic acid was prepared from 4-cyclohexylamino-2-methyl-5-nitrobenzoic acid methyl ester (Example 151) as described for the 4-methyl derivative (Example 151). The acid was coupled to 5-hydroxy-(S)-tryptophan methyl ester hydrochloride in the usual manner and following saponification of the methyl ester and purification by preparative C18 reversed-phase HPLC, the title compound of example 154 was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448281B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-4c909ac3c4cd4b81ab207055e44c3ad8 |
| Source note | uspto-grants-2002_09 |