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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240325Generated: October 31, 2026

Semicarbazide hydrochloride → HCID 178510553, compound

https://huagongshe.com/reaction/240325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSemicarbazide hydrochlorideHCID 11236—
Reactant7-Chloro-9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrileHCID 16065773—
SolventAcetonitrileHCID 6342—
ProductHCID 178510553HCID 178510553—

Reaction Steps

A mixture of 600 mg (2.25 mmol) 17g and 329 mg (2.92 mmol) semicarbazide hydrochloride in 20 ml acetonitrile was heated 14 h under reflux. After that time, TLC indicated complete conversion of the starting product. After evaporation of the solvent, the crude product was recrystallised from aqueous ethanol, and compound 43 was obtained in slightly greenish crystals (90%). 1H-NMR (d6-DMSO, 400 MHz): δ (ppm)=7.40 (sl, 1H); 7.70 (sl, 1H); 7.71 (d, J=8 Hz, 1H); 8.17 (d, J=8 Hz, 1H); 8.89 (s, 1H); 10.95 (s, 1H). ESI+MS: calcd for C14H6ClN7O: 323.70; found: 324 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648076B2
Source datasetuspto-grants-2014_02
ORD IDord-dcc7dd220a3f4b4b97eec03beb8417d4
Source noteuspto-grants-2014_02