N-(3-benzoylthiopropanoyl)-L-alanine → N-(3-Sulfanylpropanoyl)-L-leucine
Reaction equation
C([S:9][CH2:10][CH2:11][C:12]([NH:14][C@H:15]([C:20]([OH:22])=[O:21])[CH2:16][CH:17]([CH3:19])[CH3:18])=[O:13])(=O)C1C=CC=CC=1.C(SCCC(N[C@H](C(O)=O)C)=O)(=O)C1C=CC=CC=1>>[SH:9][CH2:10][CH2:11][C:12]([NH:14][C@H:15]([C:20]([OH:22])=[O:21])[CH2:16][CH:17]([CH3:19])[CH3:18])=[O:13]Participants
3
Procedure
By substituting N-(3-benzoylthiopropanoyl)-L-leucine (6.46 g.) for the N-(3-benzoylthiopropanoyl)-L-alanine in the procedure of Example 2, 2.75 g. of N-(3-mercaptopropanoyl)-L-leucine are obtained, m.p. 131°-132°. This material is recrystallized from acetonitrile.
Sources & evidence
- ORD record
- ord-8aa5823fa7184b2cb5ffd10599e64f16
- Source dataset
- uspto-grants-1982_07
- Patent number
- US04339600
Reaction notes
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