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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035781Generated: October 29, 2026

1,4-Dimercapto-2,3-butanediol → HCID 42598894, compound

https://huagongshe.com/reaction/1035781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dimercapto-2,3-butanediolHCID 19001—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantHCID 21822186HCID 21822186—
ReactantHCID 86647895HCID 86647895—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 42598894HCID 4259889423.7%

Reaction Steps

The 1-{6-[(6-methoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-yl}-3-[2-(pyrrolidin-1-yl)ethyl]urea was prepared according to the method described in Example 17a, but using 547 mg of 1-[2-(pyrrolidin-1-yl)ethyl]-3-(6-sulphanyl-1,3-benzothiazol-2-yl)urea, 25 cm3 of degassed ethanol, 8 mg of potassium dihydrogen phosphate in 0.2 cm3 of water, 787 mg of DL-dithiothreitol and 313 mg of 3-chloro-6-methoxy[1,2,4]triazolo[4,3-b]pyridazine. 189 mg of 1-{6-[(6-methoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-yl}-3-[2-(pyrrolidin-1-yl)ethyl]urea are thus obtained in the form of a white powder, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546393B2
Source datasetuspto-grants-2013_10
ORD IDord-bfc74dc7437a4772bf48fdcc38e29036
Source noteuspto-grants-2013_10