HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthylalanine → N-[(1S)-2-[[(5S)-5-[(4-amino-3-chloro-phenyl)sulfonyl-isobutyl-amino]-6-hydroxy-hexyl]amino]-1-(2-naphthylmethyl)-2-oxo-ethyl]morpholine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthylalanine | HCID 185915 | — |
| Reactant | N-[(1S)-2-[[(5S)-5-[(4-amino-3-chloro-phenyl)sulfonyl-isobutyl-amino]-6-hydroxy-hexyl]amino]-1-(1-naphthylmethyl)-2-oxo-ethyl]morpholine-4-carboxamide | HCID 513966 | — |
| Reactant | 1-Naphthyl-L-alanine | HCID 2724883 | — |
| Reactant | (2s)-2-[(Morpholine-4-carbonyl)-amino]-3-naphthalen-1-yl-propionic acid | HCID 12986165 | — |
| Reactant | (2s)-2-[(Morpholine-4-carbonyl)-amino]-3-naphthalen-2-yl-propionic acid | HCID 67532430 | — |
| Product | N-[(1S)-2-[[(5S)-5-[(4-amino-3-chloro-phenyl)sulfonyl-isobutyl-amino]-6-hydroxy-hexyl]amino]-1-(2-naphthylmethyl)-2-oxo-ethyl]morpholine-4-carboxamide | HCID 513973 | 25% |
Reaction Steps
This derivative was prepared from (1S)-4-amino-N-(5-amino-1-hydroxymethyl-pentyl)-3-chloro-N-isobutyl-benzenesulfonamide (XII) (example 44, step B) as described in general procedure B using (2S)-2-[(morpholine-4-carbonyl)-amino]-3-naphthalen-2-yl-propionic acid. The latter derivative was prepared from L-2-naphthylalanine as described for the preparation of (2S)-2-[(morpholine-4-carbonyl)-amino]-3-naphthalen-1-yl-propionic acid from L-1-naphthylalanine. The final product was obtained in 25% yield (51 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06632816B1 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-75f1524aec05426aaab892a003fe58d0 |
| Source note | uspto-grants-2003_10 |