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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633509Generated: October 26, 2026

Ethanol → 6-[(6-Ethoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-amine

https://huagongshe.com/reaction/633509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1,4-Dimercapto-2,3-butanediolHCID 19001—
Reactant2-Amino-6-thiocyanato-1,3-benzothiazoleHCID 81600—
ReactantHCID 67524522HCID 67524522—
CatalystMonobasic potassium phosphateHCID 516951—
SolventWaterHCID 962—
Product6-[(6-Ethoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-amineHCID 4259889580.3%

Reaction Steps

The 6-[(6-ethoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-amine was prepared according to the method described in Example 17a, but using 587 mg of 2-amino-1,3-benzothiazol-6-yl thiocyanate (commercial), 20 cm3 of degassed ethanol, 13 mg of potassium dihydrogen phosphate in 0.2 cm3 of water, 1.31 g of DL-dithiothreitol and 562 mg of 3-chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazine. 783 mg of 6-[(6-ethoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-amine are thus obtained in the form of a whitish powder, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321777B2
Source datasetuspto-grants-2016_04
ORD IDord-542b229f19334344b5bc98c618b6372f
Source noteuspto-grants-2016_04