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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907526Generated: October 25, 2026

Water → 1-(4-Chloro-[1,2,5]thiadiazol-3-yl)-3,5-dimethyl-piperazine

https://huagongshe.com/reaction/907526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,6-DimethylpiperazineHCID 66056—
Reactant3,4-Dichloro-1,2,5-thiadiazoleHCID 79804—
SolventDimethylformamideHCID 6228—
Product1-(4-Chloro-[1,2,5]thiadiazol-3-yl)-3,5-dimethyl-piperazineHCID 5901394997%

Reaction Conditions

Temperature100 °C

Reaction Steps

2,6-Dimethyl-piperazine (8.1 g, 71 mmol) was heated to 100° C. in DMF (8.0 ml). 3,4-Dichloro-1,2,5-thiadiazole (3.3 ml, 35 mmol) was added and the mixture stirred at 100° C. for 3-4 h. The reaction mixture was poured into H2O and extracted with EtOAc (4×). The combined EtOAc extractions were washed with sat'd NaHCO3 (1×), sat'd NaCl (1×), dried (Na2SO4), and concentrated in vacuo to give 7.9 g (97%) of 1-(4-chloro-[1,2,5]thiadiazol-3-yl)-3,5-dimethyl-piperazine which was used without further purification. 1H NMR (CDCl3) 3.90-3.86 (m, 2H), 3.05 (m, 2H), 2.52 (m, 2H), 1.12 (d, 6H) ppm. LC-MS (MH+)=233.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013156B2
Source datasetuspto-grants-2011_09
ORD IDord-3ea7e018ba6f4de69e625dffc4e04115
Source noteuspto-grants-2011_09