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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110042Generated: November 1, 2026

Ammonium formate → HCID 23068987, compound

https://huagongshe.com/reaction/2110042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 23068946HCID 23068946—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 23068987HCID 23068987—

Reaction Steps

5-Bromo-7,8-dimethyl-2H,4H-benzo[e]1,2,4-thiadiazine-1,1,3-trione (5.27 g, 17.3 mmol) was suspended in methanol (60 mL), and then ammonium formate (5.45 g, 86.5 mmol, 5 eq) was added and nitrogen substitution was performed. Next, 10% palladium-carbon powder (1.84 g, 1.73 mmol, 10 mol %) was added and the mixture was heated to reflux for 4 hours. The reaction mixture was cooled to room temperature and filtered through celite. The filtrate was cooled on ice and the precipitated crystals were filtered out and dried to obtain 7,8-dimethyl-2H, 4H-benzo[e]1,2,4-thiadiazine-1,1,3-trione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517875B2
Source datasetuspto-grants-2009_04
ORD IDord-dd5e4a9cf8ca43959921f5e9ddde7c47
Source noteuspto-grants-2009_04