L-(+)-Cysteine → Butanol acetic acid water
Reaction equation
[C:1]1(=O)N[C:4](=[O:6])[CH:3]=[CH:2]1.N[C@H:9]([C:12]([OH:14])=[O:13])CS>>[CH2:4]([OH:6])[CH2:3][CH2:2][CH3:1].[C:12]([OH:14])(=[O:13])[CH3:9].[OH2:6]Participants
3
Procedure
A stable thioether bond forms when a sulfhydryl-containing peptide is reacted with the maleimide bearing intercalator as shown in Scheme 3 above, a sulfhydryl group may be attached to the N-terminal of the peptide with the reagent succinimidyl 3(2-pyridyldithio) propionate (Carlsson, J., et al., Biochem. 173:723 (1978)). Alternatively, the peptide may be synthesized with a cysteine residue at the appropriate location. The synthesis is robust and provides an overall yield of about 15%.
Workup
- customprovides an overall yield of about 15%
Sources & evidence
- ORD record
- ord-5ded69935b394aadb20c6be95434929b
- Source dataset
- uspto-grants-1997_08
- Patent number
- US05661025
Reaction notes
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