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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045768Generated: October 31, 2026

Ethyl orthoformate → HCID 178480782, compound

https://huagongshe.com/reaction/1045768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant5-Bromo-2-(4-methyl-1-piperazinyl)-3,4-pyridinediamineHCID 58446990—
ProductHCID 178480782HCID 17848078279%

Reaction Conditions

Temperature130 °C

Reaction Steps

A 100 mL round bottom flask was charged with 5-bromo-2-(4-methylpiperazin-1-yl)pyridine-3,4-diamine (1.1 g, 3.8 mmol) and triethyl orthoformate (20 mL). The resulting mixture was stirred at 130° C. for 1 h. Reaction progress was monitored by TLC (EtOAc/petroleum ether=2:1). Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in EtOAc (50 mL) and washed with brine (20 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 10-40% EtOAc in CH2Cl2, to afford 0.9 g (79%) of the product as a white solid. MS m/z: 296 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569300B2
Source datasetuspto-grants-2013_10
ORD IDord-a1764a9570b245dfbb264b97a248384a
Source noteuspto-grants-2013_10