Homoveratrylamine → HCID 3939109, compound
Reaction equation
[C:1]12([C:11](Cl)=[O:12])[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[CH2:14]([NH2:26])[CH2:15][C:16]1[CH:25]=[CH:24][C:21]([O:22][CH3:23])=[C:18]([O:19][CH3:20])[CH:17]=1.C(N(CC)CC)C>C(OCC)(=O)C.C(OCC)C>[CH3:20][O:19][C:18]1[CH:17]=[C:16]([CH2:15][CH2:14][NH:26][C:11]([C:1]23[CH2:10][CH:5]4[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]4)[CH2:2]2)[CH2:8]3)=[O:12])[CH:25]=[CH:24][C:21]=1[O:22][CH3:23]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Subject 2.0 g. of adamantane carboxylic acid chloride 1.8 g. (10.0 mmoles) of homoveratrylamine and 5.0 ml. of triethylamine to the process of Example 11. Crystallize the residue obtained thereby from an ethyl acetate-ethyl ether mixture to obtain the title product, m.p. 132°-133°C.
Workup
- customCrystallize the residue
- customobtained
Sources & evidence
- ORD record
- ord-7fef49c72ddd40c7aa0853065e53c148
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03944675
Reaction notes
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