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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247586Generated: October 31, 2026

Hydrochloric Acid → 4-(Isoquinoline-5-sulfonyl)piperazine-1-carboximidamide

https://huagongshe.com/reaction/247586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant5-Isoquinolinesulfonyl chlorideHCID 3371655—
Reactant1052089-53-8HCID 15594677—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(Isoquinoline-5-sulfonyl)piperazine-1-carboximidamideHCID 1441651487.9%

Reaction Steps

In 30 ml of water was dissolved 3.9 g of 1-amidinopiperazine sulfate, and 60 ml of tetrahydrofuran solution containing 4.1 g of 5-isoquinolinesulfonyl chloride and 1N sodium hydroxide was added dropwise under cooling with ice so that the pH of the solution maintain the range from 8 to 8.5. After the dropwise addition, the mixture solution was stirred for one hour. The crystalline residue was discarded, and the pH of the aqueous layer was adjusted to 1 with an aqueous diluted hydrochloric acid solution. The crystalline residue was discarded, and the pH of the aqueous layer was adjusted to 13 with a 5N aqueous sodium hydroxide solution. The crystals precipitated were separated by filtration, and the crystalline residue obtained was dissolved with an aqueous diluted hydrochloric acid solution. The pH of the solution was adjusted to 13.5 with a 2N aqueous sodium hydroxide solution. The crystals precipitated were separated by filtration, the crystalline residue was washed with water, methanol and ethylether and condensed to dryness to give 4.84 g of 4-amidino-1-(5-isoquinolinesulfonyl)piperazine, i.e., Compound (44) in a yield of 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04709032
Source datasetuspto-grants-1987_11
ORD IDord-46ae07d49c6a4653a8c870adabd5d4e9
Source noteuspto-grants-1987_11