Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49305Generated: October 29, 2026

Hydrochloric Acid → HCID 20634926, compound

https://huagongshe.com/reaction/49305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 20634972HCID 20634972—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
ProductHCID 20634926HCID 2063492682%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1,4-bis[5-(4-benzyloxycarbonylamino-3,5-dimethoxyphenyl)-2-pyridyl]hexahydro-1,4-diazepine (120.0 mg, 0.140 mmol) in acetic acid (2.0 mL) was added 10% palladium on charcoal (24.0 mg), and the resulting mixture was stirred at 50° C. for 1.5 hours under hydrogen. Insoluble materials were removed by filtration through Celite, and the filtrate was concentrated under reduced pressure. A solution of the residue in chloroform was washed with saturated aqueous sodium hydrogencarbonate and brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. To a solution of the residue in chloroform (5.0 mL) a 4.0 M solution of hydrogen chloride in ethyl acetate (0.14 mL, 0.56 mmol), and the resulting mixture was concentrated under reduced pressure. Ethanol (5.0 mL) was added to the residue, and the resulting mixture was concentrated under reduced pressure. Diethyl ether was added to the residue, and the resulting precipitate was collected by filtration to yield the title compound as a pale brown amorphous powder (84.0 mg, yield: 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706703B2
Source datasetuspto-grants-2004_03
ORD IDord-a0813cd016674920b603ebd8e4f372ef
Source noteuspto-grants-2004_03