HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702331Generated: October 29, 2026
Tetrafluoro-m-phenylenediamine dihydrochloride → HCID 178482521, compound
https://huagongshe.com/reaction/1702331
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole | HCID 665568 | — |
| Reactant | 3,4-Dimethoxy-1,2,5-thiadiazole 1,1-dioxide | HCID 12230538 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178482521 | HCID 178482521 | — |
Reaction Steps
To a well stirred suspension of 3,4-dimethoxy-1,2,5-thiadiazole 1,1-dioxide (2.5 g; 14.0 mmoles) in 250 ml of dry methanol that had been cooled to 2° in an ice-water bath was added dropwise over a period of 25 minutes a solution of 2-[(5-methyl-1-H-imidazol-4-yl)methylthio]ethylamine (from the dihydrochloride, 3.42 g; 14.0 mmoles) in 25 ml of methanol. After stirring at 2° for 20 minutes, anhydrous methylamine was bubbled into the solution for 6 minutes and stirring was continued at ambient temperature for 30 minutes. The reaction mixture was evaporated under reduced pressure and the residue was placed on 50 g of silica gel and chromatographed by gradient elution using methylene chloride-methanol. The appropriate fractions were combined to give 3.2 g of the title compound. Additional purification of the product using column chromatography gave an analytical sample of the title compound as an amorphous solid, mp 98°-110°. The NMR spectrum (100 MHz) in d6 dimethyl sulfoxide gave the following resonances δ: 7.46 (s, 1H); 3.70 (s, 2H); 2.53 (t, 2H); 2.86 (s, 3H); 2.72 (t, 2H); 2.15 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04380639 |
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| Source dataset | uspto-grants-1983_04 |
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| ORD ID | ord-6634572a24b84b0692f12c1f23e9a6c1 |
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| Source note | uspto-grants-1983_04 |
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