Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702351Generated: October 29, 2026

Tetrafluoro-m-phenylenediamine dihydrochloride → HCID 178457004, compound

https://huagongshe.com/reaction/1702351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
ReactantPropargylamineHCID 239041—
Reactant3,4-Dimethoxy-1,2,5-thiadiazole 1,1-dioxideHCID 12230538—
Reactant2-[4-(2-Aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]guanidineHCID 178512723—
SolventMethanolHCID 887—
ProductHCID 178457004HCID 178457004—

Reaction Steps

A solution of 2-[(2-guanidinothiazol-4-yl)methylthio]ethylamine (from the dihydrochloride, 3.42 g; 11.2 mmoles) in 25 ml of methanol was added to a well stirred cold (8°) suspension of 3,4-dimethoxy-1,2,5-thiadiazole 1,1-dioxide (2.0 g; 11.2 mmoles) in 200 ml of methanol. After 15 minutes at 8°-10°, the solution was cooled to 1° in an ice-bath and a solution of 6.0 ml 2-propynylamine in 15 ml of methanol was added. The ice-bath was removed and stirring was continued for 15 minutes. The reaction mixture was evaporated under reduced pressure and the residue placed on 50 g of silica gel and chromatographed using a gradient elution of methylene chloride-methanol. Two of the fractions yielded crystalline product (1.74 g) from methanol. The product was dissolved in hot methanol, filtered through Celite, cooled and filtered to yield the title compound, mp 176°-178°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380639
Source datasetuspto-grants-1983_04
ORD IDord-fed2957dabc24caaae02a87d04e0169c
Source noteuspto-grants-1983_04