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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659751Generated: October 26, 2026

Piperazine Dihydrochloride → Irbesartan

https://huagongshe.com/reaction/659751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazine DihydrochlorideHCID 8893—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AzideHCID 33557—
Reactant4'-((2-Butyl-4-oxo-1,3-diazaspiro(4.4)non-1-ene-3-yl)methyl)(1,1'-biphenyl)-2-carbonitrileHCID 9843116—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductIrbesartanHCID 374998%

Reaction Steps

A mixture of 2-n-butyl-3-[(2′-cyanobiphenyl-4-yl)methyl]-1,3-diazaspiro-[4,4]-non-1-en-4-one (10 g), sodium azide (7.7 g) and piperazine dihydrochloride (7.5 g) in N,N-dimethylformamide (30 ml) was refluxed for 7 hours under stirring. The reaction was cooled to room temperature and 20 ml water was added. The reaction mixture was adjusted to pH of about 12 using 10% NaOH solution. The alkaline solution was washed with toluene (15 ml) and the aqueous phase was neutralized to pH of 6.5 using concentrated HCl. The resulting suspension was stirred for 3 hours at room temperature and filtered to obtain irbesartan (5.8 g, 98% purity by HPLC). Recrystallization of the Product using ethanol results in 5.2 g of irbesartan with 99.94% purity and content of the impurity 2-n-butyl-3-[(2′-carboxamidobiphenyl-4-yl)methyl]-1,3-diazaspiro-[4,4]-non-1-en-4-one: 0.07%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080670B2
Source datasetuspto-grants-2011_12
ORD IDord-a87991bb691b4f3d9269906fa7cf021a
Source noteuspto-grants-2011_12