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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38133Generated: October 26, 2026

Hydrazine, dihydrochloride → HCID 178428372, compound

https://huagongshe.com/reaction/38133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, dihydrochlorideHCID 17548—
Reactant(5-Chloro(2-thienyl))-n-({[4-(5-chloro-1,3-dioxobenzo[c]azolin-2-yl)-3-methylphenyl]amino}thioxomethyl)carboxamideHCID 20800070—
SolventDimethylformamideHCID 6228—
ProductHCID 178428372HCID 17842837214.2%

Reaction Steps

To a suspension of (5-chloro(2-thienyl))-N-({[4-(5-chloro-1,3-dioxobenzo[c]azolin-2-yl)-3-methylphenyl]amino}thioxomethyl)carboxamide (15 mg, 0.030 mmol) and hydrazine dihydrochloride (4 mg, 0.038 mmol) in DMF (0.3 mL) was added HgO (7 mg, 0.032 mmol). The reaction was stirred at room temp for 17 hr, and HPLC purified to give the desired product 5-chloro-2-(4-{[5-(5-chloro(2-thienyl))(4H-1,2,4-triazol-3-yl)]amino}-2-methylphenyl)benzo[c]azoline-1,3-dione (2 mg) (ES-MS (M+H)+=470, 472) and the aminoguanidine intermediate N-((1E)-2-aza-1-{[4-(5-chloro-1,3-dioxobenzo[c]azolidin-2-yl)-3-methylphenyl]amino}-2-aminovinyl)(5-chloro(2-thienyl))carboxamide (2 mg) ES-MS (M+H)+=488, 490 (2Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524721B2
Source datasetuspto-grants-2013_09
ORD IDord-3dbd1661402841ceb13eab318ed44ef4
Source noteuspto-grants-2013_09