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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987975Generated: October 30, 2026

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

https://huagongshe.com/reaction/987975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphthylalanineHCID 185915—
ReactantN-[(1S)-2-[[(5S)-5-[(4-amino-3-chloro-phenyl)sulfonyl-isobutyl-amino]-6-hydroxy-hexyl]amino]-1-(1-naphthylmethyl)-2-oxo-ethyl]morpholine-4-carboxamideHCID 513966—
Reactant1-Naphthyl-L-alanineHCID 2724883—
Reactant(2s)-2-[(Morpholine-4-carbonyl)-amino]-3-naphthalen-1-yl-propionic acidHCID 12986165—
Reactant(2s)-2-[(Morpholine-4-carbonyl)-amino]-3-naphthalen-2-yl-propionic acidHCID 67532430—
ProductN-[(1S)-2-[[(5S)-5-[(4-amino-3-chloro-phenyl)sulfonyl-isobutyl-amino]-6-hydroxy-hexyl]amino]-1-(2-naphthylmethyl)-2-oxo-ethyl]morpholine-4-carboxamideHCID 51397325%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06632816B1
Source datasetuspto-grants-2003_10
ORD IDord-75f1524aec05426aaab892a003fe58d0
Source noteuspto-grants-2003_10