3-Ethoxy-4-ethoxycarbonylphenylacetic acid → HCID 10814522, compound
Reaction equation
[CH:1]1([CH2:4][CH:5]([NH2:18])[C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[N:12]2[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]2)[CH2:3][CH2:2]1.[CH2:19]([O:21][C:22]1[CH:23]=[C:24]([CH2:33][C:34](O)=[O:35])[CH:25]=[CH:26][C:27]=1[C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH3:20]>>[CH2:19]([O:21][C:22]1[CH:23]=[C:24]([CH2:33][C:34]([NH:18][CH:5]([CH2:4][CH:1]2[CH2:3][CH2:2]2)[C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[N:12]2[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]2)=[O:35])[CH:25]=[CH:26][C:27]=1[C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH3:20]Participants
3
Procedure
Prepared analogously to Example 47 from α-cyclopropylmethyl-2-piperidino-benzylamine and 3-ethoxy-4-ethoxycarbonyl-phenylacetic acid.
Sources & evidence
- ORD record
- ord-7f91cc1b3f444fac82e4e5ff4936b96f
- Source dataset
- uspto-grants-2001_01
- Patent number
- USRE037035E1
Reaction notes
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