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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702316Generated: October 29, 2026

Tetrafluoro-m-phenylenediamine dihydrochloride → 3-Amino-4-[(3-{3-[(piperidin-1-yl)methyl]phenoxy}propyl)amino]-1H-1lambda~4~,2,5-thiadiazol-1-one

https://huagongshe.com/reaction/1702316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
Reactant3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amineHCID 10220561—
Reactant3,4-Dimethoxy-1,2,5-thiadiazole 1-oxideHCID 12913947—
SolventMethanolHCID 887—
Product3-Amino-4-[(3-{3-[(piperidin-1-yl)methyl]phenoxy}propyl)amino]-1H-1lambda~4~,2,5-thiadiazol-1-oneHCID 5486883—

Reaction Steps

A solution of 3-(3-piperidinomethylphenoxy)propylamine (from the dihydrochloride, 4.0 g; 12.4 mmoles) in 40 ml of methanol was added dropwise over a period of 50 minutes to a solution of 3,4-dimethoxy-1,2,5-thiadiazole 1-oxide (2.01 g; 12.4 mmoles) in 200 ml of methanol that had been cooled to 0° in an ice-water bath. After 15 minutes, anhydrous ammonia was bubbled into the solution for 5 minutes and the solution then was stirred at ambient temperature for 17 hours. The reaction mixture was evaporated under reduced pressure and the residue chromatographed by flash chromatography on 100 g of silica gel (230-400 mesh) using methanol-acetonitrile. The appropriate fractions were combined and evaporated to give 4.18 g of product. Recrystallization from 95% aqueous ethanol yielded the title compound, mp 155°-157° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380638
Source datasetuspto-grants-1983_04
ORD IDord-9baeb7a60f57421eb752ac4ebc865c75
Source noteuspto-grants-1983_04