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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390424Generated: October 26, 2026

5-Amino-1,2,4-thiadiazole → N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-chloropyrimidin-2-ylthio)phenyl)-3,3,3-trifluoropropanamide

https://huagongshe.com/reaction/390424

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-1,2,4-thiadiazoleHCID 290274—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantN-(4-(4,6-dichloropyrimidin-2-ylthio)phenyl)-3,3,3-trifluoropropanamideHCID 59352891—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductN-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-chloropyrimidin-2-ylthio)phenyl)-3,3,3-trifluoropropanamideHCID 5945031734%

Reaction Steps

To a round bottom flask was added N-(4-(4,6-dichloropyrimidin-2-ylthio)phenyl)-3,3,3-trifluoropropanamide (350 mg, 0.9 mmol), 1,2,4-thiadiazole-5-amine (100 mg, 0.9 mmol), xanthphos (50 mg, 0.1 mmol), Pd2 dba3 (50 mg, 0.05 mmol), NaCO3 (150 mg, 1.5 mmol) and dioxane(10 cm). The mixture was flushed with nitrogen and then brought to reflux for 2 hours. The mixture was filtered, partitioned between ethylacetate and bicarbonate. The organic layer was dried with magnesium sulfate, and concentrated to an oil, which was purified by column chromatography to yield the product as a yellow solid (127 mg, 34%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383633B2
Source datasetuspto-grants-2013_02
ORD IDord-b08aecb389014c2983dc64e972c5b12a
Source noteuspto-grants-2013_02