Methyl 3-(4-aminophenyl)propanoate → HCID 56639921, compound
Reaction equation
[CH3:1][O:2]/[N:3]=[C:4](/[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)\[CH2:5][O:6][C:7]1[CH:14]=[CH:13][C:10]([CH:11]=O)=[CH:9][CH:8]=1.[NH2:21][C:22]1[CH:27]=[CH:26][C:25]([CH2:28][CH2:29][C:30]([O:32]C)=[O:31])=[CH:24][CH:23]=1>>[CH3:1][O:2]/[N:3]=[C:4](/[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)\[CH2:5][O:6][C:7]1[CH:14]=[CH:13][C:10]([CH2:11][NH:21][C:22]2[CH:23]=[CH:24][C:25]([CH2:28][CH2:29][C:30]([OH:32])=[O:31])=[CH:26][CH:27]=2)=[CH:9][CH:8]=1Participants
3
Procedure
Compound 4 was synthesized from 4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzaldehyde and methyl 3-(4-aminophenyl)propanoate by following the procedure described in Scheme 3.
Sources & evidence
- ORD record
- ord-660b2b8409cc403ba4e43e37851d6319
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09278915B2
Reaction notes
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