2,4-Diethoxybenzoic acid → HCID 22494321, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:12]=[C:11]([O:13][CH2:14][CH3:15])[CH:10]=[CH:9][C:5]=1[C:6]([OH:8])=O)[CH3:2].C(OC([NH:23][CH2:24][C:25]1[CH:26]=[C:27]([CH2:33][CH:34]([O:38][CH:39]([CH3:41])[CH3:40])[C:35]([O-:37])=[O:36])[CH:28]=[CH:29][C:30]=1[O:31][CH3:32])=O)(C)(C)C>>[CH2:1]([O:3][C:4]1[CH:12]=[C:11]([O:13][CH2:14][CH3:15])[CH:10]=[CH:9][C:5]=1[C:6]([NH:23][CH2:24][C:25]1[CH:26]=[C:27]([CH2:33][CH:34]([O:38][CH:39]([CH3:41])[CH3:40])[C:35]([OH:37])=[O:36])[CH:28]=[CH:29][C:30]=1[O:31][CH3:32])=[O:8])[CH3:2]Participants
3
Procedure
Using 2,4-diethoxybenzoic acid and 3-[3-([(tert-butoxycarbonyl)amino]methyl)-4-methoxyphenyl)-2-isopropoxypropanoate, 3-(3-[(2,4-diethoxybenzoyl)amino]methyl-4-methoxyphenyl)-2-isopropoxypropanoic acid was obtained in the same method as in Example 38).
Sources & evidence
- ORD record
- ord-6d9e69e6311d4ddc97a1c95c0dc3eb50
- Source dataset
- uspto-grants-2005_04
- Patent number
- US06884821B1
Reaction notes
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