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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830172Generated: November 1, 2026

Benzyl 4-azido-3-hydroxyazepane-1-carboxylate → 4-(4-Morpholin-4-yl-4-oxo-2-benzylsulfonylmethyl-butyrylamino)-3-oxo-azepane-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1830172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-azido-3-hydroxyazepane-1-carboxylateHCID 10661164—
Reactant4-Morpholin-4-yl-4-oxo-2-benzylsulfonylmethyl-butyric acidHCID 22053987—
Product4-(4-Morpholin-4-yl-4-oxo-2-benzylsulfonylmethyl-butyrylamino)-3-oxo-azepane-1-carboxylic acid benzyl esterHCID 21031020—

Reaction Steps

The crude 4-amino-3-hydroxy-azepane-1-carboxylic acid benzyl ester was coupled to 4-morpholin-4-yl-4-oxo-2-benzylsulfonylmethyl-butyric acid and oxidized, as described above, to yield 4-(4-morpholin-4-yl-4-oxo-2-benzylsulfonylmethyl-butyrylamino)-3-oxo-azepane-1-carboxylic acid benzyl ester; 1H NMR: (DMSO) 8.46–8.42 (m, 1H), 7.44–7.24 (m, 10H), 5.18–5.04 (m, 2H), 4.52–4.33 (m, 4H), 4.04–3.76 (m, 2H), 3.58–3.30 (m, 11H), 3.11–3.03 (m, 1H), 2.96–2.78 (m, 1H), 2.72–2.57 (m, 1H), 1.84–1.55 (m, 4H); MS: (M+H)+ 600.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064123B1
Source datasetuspto-grants-2006_06
ORD IDord-a24dc051f63742269ed454648dbf9801
Source noteuspto-grants-2006_06