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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059447Generated: November 2, 2026

Hydrochloric Acid → (10H-Pyrazino[2,3-b][1,4]benzothiazin-8-yl)acetamidine

https://huagongshe.com/reaction/1059447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
Reactant10H-Pyrazino[2,3-b][1,4]benzothiazine-8-acetonitrileHCID 18670212—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product(10H-Pyrazino[2,3-b][1,4]benzothiazin-8-yl)acetamidineHCID 1867038238.6%

Reaction Steps

2.68 g of ammonium chloride was added to 20 ml of dry toluene in a nitrogen atmosphere. Then 36.5 ml of a 15% solution of trimethylaluminum in n-hexane was added thereto under stirring and ice-cooling. The reaction mixture was brought back to room temperature and 70 ml of dry toluene was further added. The resulting mixture was subjected to ultrasonication until the ammonium chloride disappeared completely. A 60 ml portion of the solution thus obtained was taken and 1.5 g of (10H-pyrazino[2,3-b][1,4]benzothiazin-8-yl)acetonitrile was added thereto. The obtained mixture was heated under reflux for 18 hours. After bringing back to room temperature, the reaction mixture was distributed into ethyl acetate and dilute hydrochloric acid and repeatedly extracted with water. The aqueous layer was washed with methylene chloride and the solvent contained in the solution was eliminated under reduced pressure. The obtained residue was purified by High-porous gel column chromatography (CHP20, mfd. by Mitsubishi Chemical Industries, Ltd., 75-15μ) (eluted with water/methanol) to thereby give 620 mg of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-5d900e6851c54255a68a5d1c927e1b03
Source noteuspto-grants-2003_02