Glycine → L-Methionylglycine
Reaction equation
[NH2:1][C@H:2]([C:7]([OH:9])=O)[CH2:3][CH2:4][S:5][CH3:6].[NH2:10][CH2:11][C:12]([OH:14])=[O:13]>O>[NH2:1][C@H:2]([C:7]([NH:10][CH2:11][C:12]([OH:14])=[O:13])=[O:9])[CH2:3][CH2:4][S:5][CH3:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared according to the procedures of Example 1A and B above by replacing DL-methionine with L-methionine (Aldrich Chemical Co., Beil. 4(2),938). The title compound had a melting point of 188° to 190° C (d). The compound was found to be water soluble. The product thus obtained was subjected to amino acid analysis and found to contain 49.42 mole percent glycine and 50.58 mole percent methionine.
Workup
- customThe title compound was prepared
- customThe product thus obtained
Sources & evidence
- ORD record
- ord-ec2dbd97c5644168a8e01e2b4186f3f6
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04024286
Reaction notes
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