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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640424Generated: October 31, 2026

Hydrochloric Acid → 1-(5-Bromopyridin-2-yl)-1,4-diazepane

https://huagongshe.com/reaction/1640424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1-Dimethylethyl 4-(5-bromo-2-pyridinyl)-1,4-diazepane-1-carboxylateHCID 60209566—
SolventEthanolHCID 702—
SolventIsopropanolHCID 3776—
Solvent1,4-DioxaneHCID 31275—
Product1-(5-Bromopyridin-2-yl)-1,4-diazepaneHCID 16784733117.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

6 ml of a solution of hydrogen chloride (6N) in isopropanol are added to a solution of 1.63 g (4.4 mmol) of 1,1-dimethylethyl 4-(5-bromo-2-pyridyl)-1,4-diazepane-1-carboxylate, obtained in step 11.1, in 12 ml of dioxane and 4 ml of ethanol. This reaction mixture is maintained at 70° C. for 3 hours. The mixture is allowed to cool to room temperature and is then concentrated under reduced pressure. 1.32 g of a white solid are obtained after crystallization from acetone. These crystals are taken up in 10 ml of dichloromethane and the reaction medium is basified to pH=14, by adding 28% ammonia solution. The organic phase is recovered by filtration through a hydrophobic cartridge and the filtrate is concentrated under reduced pressure. 0.96 g of product is obtained in the form of an oil, and is used without further purification in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114866B2
Source datasetuspto-grants-2012_02
ORD IDord-5c6a86dd77024bb7abecc505e8c77aaa
Source noteuspto-grants-2012_02