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HRID 322041Erstellt: 24. Oktober 2026

3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamide → 3-Benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetra-hydro-4-oxo-5-[[2'-[(t-butoxycarbonylamino)methyl]-[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]-butanamide

https://huagongshe.com/de/reaction/322041

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamideHCID 20641421—
Edukt2'-[(t-Butoxycarbonylamino)methyl]-1,1-biphenyl-4-methanolHCID 22008472—
Produkt3-Benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetra-hydro-4-oxo-5-[[2'-[(t-butoxycarbonylamino)methyl]-[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]-butanamideHCID 20641423—

Reaktionsschritte

The product of Step B is prepared from 3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamide (Step A) and 2′-[(t-butoxycarbonylamino)methyl]-1,1′-biphenyl-4-methanol, methanesulfonate ester (Example 1, Step G) according to the procedure for Example 1, Step H.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211174B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-42dc8f2981ef4db187b6a59d56bd0aa6
Quellennotizuspto-grants-2001_04