Amantadine → HCID 67829987, compound
Reaction equation
C([O:4][C:5]1[CH:6]=[C:7]([CH:15]([CH3:21])[C:16]([O:18]CC)=O)[CH:8]=[CH:9][C:10]=1[O:11]C(=O)C)(=O)C.[NH2:22][C:23]12[CH2:32][CH:27]3[CH2:28][CH:29]([CH2:31][CH:25]([CH2:26]3)[CH2:24]1)[CH2:30]2>>[C:23]12([NH:22][C:16](=[O:18])[CH:15]([C:7]3[CH:8]=[CH:9][C:10]([OH:11])=[C:5]([OH:4])[CH:6]=3)[CH3:21])[CH2:30][CH:29]3[CH2:28][CH:27]([CH2:26][CH:25]([CH2:31]3)[CH2:24]1)[CH2:32]2Participants
3
Procedure
Ethyl 3,4-diacetoxyphenylpropionate and 1-aminoadamantane were used to obtain N-Adamantyl-3,4-dihydroxyphenylpropionamide by carrying out the same procedures as described in Example 1.
Sources & evidence
- ORD record
- ord-b29282a227d949dd816c37f9b0225dd5
- Source dataset
- uspto-grants-1993_08
- Patent number
- US05232923
Reaction notes
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