Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095537Generated: October 31, 2026

Potassium bisulfate → rac-(1-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-4-(1-hydroxymethyl-3-oxo-3-piperidin-1-yl-propyl)-[1,4]diazepan-5-one)

https://huagongshe.com/reaction/2095537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bisulfateHCID 516920—
ReactantLithium borohydrideHCID 4148881—
Reactant2-{4-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-7-oxo-[1,4]diazepan-1-yl}-4-oxo-4-piperidin-1-yl-butyric acid methyl esterHCID 67074068—
SolventEthanolHCID 702—
Productrac-(1-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-4-(1-hydroxymethyl-3-oxo-3-piperidin-1-yl-propyl)-[1,4]diazepan-5-one)HCID 5823209897.2%

Reaction Steps

A cooled (0° C.) solution of 0.150 g (0.29 mmol) of 2-{4-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-7-oxo-[1,4]diazepan-1-yl}-4-oxo-4-piperidin-1-yl-butyric acid methyl ester in 3.7 ml of EtOH was treated with 0.013 g (0.59 mmol) of LiBH4 (in 3 portions during 48 h until to the end of the reaction). The mixture was stirred at RT for 48 h, cooled to 0° C. and aqueous 10% KHSO4 solution was slowly added. The mixture was partitioned between aqueous saturated NaHCO3/EtOAc (3×). The organic phases were dried (Na2SO4) and evaporated to give 0.136 g (96%) of the titled compound as white foam. MS: 482.2 (MH+, 2Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445674B2
Source datasetuspto-grants-2013_05
ORD IDord-d5cf8ac1e2c7485083fbfb56d68832f6
Source noteuspto-grants-2013_05