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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095531Generated: November 1, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 1-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-4-[3-(4-hydroxy-piperidin-1-yl)-3-oxo-propyl]-[1,4]diazepan-5-one

https://huagongshe.com/reaction/2095531

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantPiperidin-4-olHCID 79341—
Reactant3-{4-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-7-oxo-[1,4]diazepan-1-yl}-propionic acidHCID 67074538—
SolventDichloromethaneHCID 6344—
Product1-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-4-[3-(4-hydroxy-piperidin-1-yl)-3-oxo-propyl]-[1,4]diazepan-5-oneHCID 58232161—

Reaction Steps

A solution of 0.100 g (0.26 mmol) of 3-{4-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-7-oxo-[1,4]diazepan-1-yl}-propionic acid (intermediate 5) and 0.032 g (0.31 mmol) of 4-hydroxypiperidine in 5 ml of dichloromethane was treated at 0° C. with 0.060 g (0.31 mmol) of EDCI. The cooling bath was allowed to come to RT and after 4 h the reaction was extracted with aqueous 10% KHSO4/EtOAc (3×). The organic phases were washed with aqueous saturated NaHCO3, 10% NaCl and dried over Na2SO4 to yield after evaporation of the solvent 0.108 g (89%) of the titled compound as white solid. MS: 468.3 (MH+, 1Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445674B2
Source datasetuspto-grants-2013_05
ORD IDord-100e0de244f74199abfc04d3669b7370
Source noteuspto-grants-2013_05