HuagongsheHuagongshe Chemistry Print Report · For research reference only
benzyl {(5S)-5-{[(5-methoxy-2-methyl-1H-indol-3-yl)acetyl]amino}-5-[5-(2-naphthyl)-1H-imidazol-2-yl]pentyl}carbamate → N-{(1S)-5-amino-1-[5-(2-naphthyl)-1H-imidazol-2-yl]pentyl}-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | benzyl {(5S)-5-{[(5-methoxy-2-methyl-1H-indol-3-yl)acetyl]amino}-5-[5-(2-naphthyl)-1H-imidazol-2-yl]pentyl}carbamate | HCID 86631539 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-{(1S)-5-amino-1-[5-(2-naphthyl)-1H-imidazol-2-yl]pentyl}-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetamide | HCID 16061501 | 94% |
Reaction Steps
A stirred solution (0.2 M) of the product from step 3 in MeOH was added to 10% Pd on carbon (17% w/w) and the heterogeneous mixture was stirred under H2 (g) at RT for the weekend. The reaction mixture was filtered through a pad of celite and washed with MeOH. Evaporation of the solvent yielded (94%) the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08080573B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-3b0fb1ab73c94be088a88a114703149c |
| Source note | uspto-grants-2011_12 |