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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095534Generated: October 31, 2026

Piperidine → (rac)-2-{4-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-7-oxo-[1,4]diazepan-1-yl}-4-hydroxy-N,N-dimethyl-butyramide

https://huagongshe.com/reaction/2095534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-4-(2-oxo-tetrahydro-furan-3-yl)-[1,4]diazepan-5-oneHCID 67074244—
Reactant(rac)-2-{4-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-7-oxo-[1,4]diazepan-1-yl}-4-hydroxy-butyric acid methyl esterHCID 67074795—
SolventEthanolHCID 702—
Product(rac)-2-{4-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-7-oxo-[1,4]diazepan-1-yl}-4-hydroxy-N,N-dimethyl-butyramideHCID 5823208843%

Reaction Steps

In analogy to the procedure described in example 3, treatment of (rac)-2-{4-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-7-oxo-[1,4]diazepan-1-yl}-4-hydroxy-butyric acid methyl ester (with 50% of the lactone, 1-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-4-(2-oxo-tetrahydro-furan-3-yl)-[1,4]diazepan-5-one) (intermediate 6) in EtOH with piperidine for 1.5 days at 60° C. and 2 days at RT gave 43% of the titled compound as light yellow foam. MS: 482.2 (MH+, 2Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445674B2
Source datasetuspto-grants-2013_05
ORD IDord-e4ae13bd14914bb58477ab2ce69367e6
Source noteuspto-grants-2013_05