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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655576Generated: November 1, 2026

Methylglyoxal → HCID 178441328, compound

https://huagongshe.com/reaction/1655576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylglyoxalHCID 880—
Reactant2-AminopropanediamideHCID 96457—
ReactantHexanal, 2-oxo-HCID 142755—
ReactantHCID 178430562HCID 178430562—
ProductHCID 178441328HCID 178441328—

Reaction Steps

2-Oxohexanal (F. Ballistreri, et al., J. Organic Chem., 53, 830 (1988) is reacted (according to the method described by F. L. Muehlmann and A. R. Day in J. American Chem. Soc., 78, 242-4(1956) substituting 2-oxohexanal for the 2-oxopropanal used in the synthesis of 5-methyl-3-hydroxypyrazine-2-carboxamide) with aminomalonamide to give 5-n-butyl-3-hydroxypyrazine-2-carboxamide. The amide is hydrolyzed with sodium hydroxide in water at 95° C. to give 5-n-butyl-3-hydroxypyrazine-2-carboxylic acid. The acid is converted to the corresponding ester with methanol and hydrochloric acid and the ester is chlorinated with phosphorous oxychloride (according to the method described by G. Dick and H. Wood in J. Chem. Soc., 1955, 1379-82) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250548
Source datasetuspto-grants-1993_10
ORD IDord-a985b5bcad5b47798258848cd8b37045
Source noteuspto-grants-1993_10