Methylglyoxal → HCID 178430698, compound
Reaction equation
Cl.[NH2:2][C@H:3]([C:5]([NH2:7])=[O:6])[CH3:4].[CH3:8][C:9]([CH:11]=O)=O>>[OH:6][C:5]1[C:3]([CH3:4])=[N:2][C:9]([CH3:11])=[CH:8][N:7]=1Participants
3
Procedure
The title-compound was prepared from alanine amide hydrochloride and pyruvic aldehyde as described by Karmas and Spoerri, J. Am. Chem. Soc., 1952, 74, 1580 m.p.=149.5°-151° C. (Lit. 146°-147° C.).
Workup
- custom=149.5°-151° C. (Lit. 146°-147° C.)
Sources & evidence
- ORD record
- ord-fe98a0a6ef854f2ca0da0edf4f173d04
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05260293
Reaction notes
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