Methanesulfonic Acid → Carnosine
Reaction equation
[NH2:1][C@H:2]([C:9]([OH:11])=[O:10])[CH2:3][C:4]1[N:8]=[CH:7][NH:6][CH:5]=1.S1[CH2:17][CH2:16][C:15](=[O:18])NC1=O.[OH-].C[N+:22](C)(C)C.CS(O)(=O)=O>>[CH:5]1[N:6]=[CH:7][NH:8][C:4]=1[CH2:3][C@H:2]([NH:1][C:15]([CH2:16][CH2:17][NH2:22])=[O:18])[C:9]([OH:11])=[O:10]Participants
5
Procedure
Starting with 1.55 g. (10 mmol) of L-histidine, 2.62 g. (20 mmol) of tetrahydro-1,3-thiazin-2,4-dione, 20% aqueous tetramethylammonium hydroxide solution to raise the pH and methanesulfonic acid to lower the pH, and following the procedure of Example 1, there was isolated 1.13 g. (50% yield) of L-carnosine.
Workup
- customthere was isolated 1.13 g
Sources & evidence
- ORD record
- ord-f44b0137363241e19cb3774ee96866d1
- Source dataset
- uspto-grants-1982_11
- Patent number
- US04359416
Reaction notes
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