Alanine, methyl ester, hydrochloride (1:1) → 2-Cycloheptanoylaminopropionic acid
Reaction equation
Cl.[NH2:2][CH:3]([C:5]([O:7]C)=[O:6])[CH3:4].[CH:9]1([C:16](Cl)=[O:17])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1>>[CH:9]1([C:16]([NH:2][CH:3]([CH3:4])[C:5]([OH:7])=[O:6])=[O:17])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1Participants
3
Procedure
The preparation is carried out analogously to the procedure of Example 7A using 20 g (143 mmol) of methyl D,L-alaninate hydrochloride and 23.02 g (143 mmol) of cycloheptanoyl chloride.
Sources & evidence
- ORD record
- ord-fac4b5e56aa94f33b8e8a13e05c827bd
- Source dataset
- uspto-grants-2005_01
- Patent number
- US06838459B1
Reaction notes
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