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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758596Generated: October 30, 2026

Tetrafluoro-m-phenylenediamine dihydrochloride → HCID 178433672, compound

https://huagongshe.com/reaction/1758596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
Reactant4-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 665568—
Reactant4-methoxy-N-[2-[(5-methyl-1H-imidazol-4-yl)methylsulfanyl]ethyl]-1,1-dioxo-1,2,5-thiadiazol-3-amineHCID 178494335—
Reactant2-[4-(2-Aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]guanidineHCID 178512723—
SolventMethanolHCID 887—
ProductHCID 178433672HCID 178433672—

Reaction Steps

To a well stirred solution at -10° of 3-{2-[(5-methyl-1H-imidazol-4-yl)methylthio]ethylamino}-4-methoxy-1,2,5-thiadiazole 1,1-dioxide [prepared from the dihydrochloride of 2-{(5-methyl-1H-imidazol-4-yl)methylthio}ethylamine (2.73 g; 11.2 mmole) by the procedure of Step A of Example 1] was rapidly added a solution of 2-[(2-guanidinothiazol-4-yl)methylthio]ethylamine (from the dihydrochloride, 3.41 g; 11.2 mmoles) [prepared according to the procedure described in South African Pat. No. 78/2129] in 35 ml of methanol. After stirring at -10° for 30 minutes, the solution was allowed to warm to ambient temperature. The reaction mixture was evaporated under reduced pressure and the residue was placed on 45 g of silica gel and chromatographed using 1 liter of methylene chloride-methanol (4:1). The appropriate fractions were combined and evaporated, and the residue (5.82 g) was placed on 80 g of aluminum oxide and chromatographed using a gradient elution of ethyl acetate-methanol. The appropriate fractions were combined, filtered through Celite and evaporated under high vacuum to yield the title compound (2.5 g) as an amorphous solid containing approximately 2/3 mole of ethyl acetate, as ascertained by the NMR spectrum (100 MHz) in d6 dimethyl sulfoxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374248
Source datasetuspto-grants-1983_02
ORD IDord-ae6ddda734724b7e9f771443931fc7d4
Source noteuspto-grants-1983_02