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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633495Generated: October 30, 2026

1,4-Dimercapto-2,3-butanediol → HCID 86707008, compound

https://huagongshe.com/reaction/633495

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dimercapto-2,3-butanediolHCID 19001—
Reactant3-chloro-6-(4-methylpiperazin-1-yl)[1,2,4]triazolo[4,3-b]pyridazineHCID 313625—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantHCID 86707009HCID 86707009—
ReactantHCID 86707010HCID 86707010—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 86707008HCID 86707008—

Reaction Steps

The 1,1-dimethylethyl (6-{[6-(4-methylpiperazin-1-yl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulphanyl}-1,3-benzothiazol-2-yl)carbamate can be prepared according to the method described in Example 17a, but using 565 mg of 1,1-dimethylethyl (6-thiocyanato-1,3-benzothiazol-2-yl)carbamate (prepared according to Example 2c), 16 cm3 of ethanol, 16 mg of potassium dihydrogen phosphate in 1.6 cm3 of water, 924 mg of DL-dithiothreitol and 505 mg of 3-chloro-6-(4-methylpiperazin-1-yl)[1,2,4]triazolo[4,3-b]pyridazine. 246 mg of 1,1-dimethylethyl (6-{[6-(4-methylpiperazin-1-yl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulphanyl}-1,3-benzothiazol-2-yl)carbamate hydrochloride are thus obtained in the form of a white solid, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321777B2
Source datasetuspto-grants-2016_04
ORD IDord-be8566d725e7414cb8896b8f39d3ebca
Source noteuspto-grants-2016_04