2,3-Dichlorobenzoic acid → HCID 73673068, compound
Reaction equation
[Cl:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[CH3:12][O:13][CH:14]1[CH2:19][CH2:18][N:17]([CH:20]([C:23]2[CH:24]=[N:25][C:26]([CH3:29])=[N:27][CH:28]=2)[CH2:21][NH2:22])[CH2:16][CH2:15]1>>[Cl:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH:22][CH2:21][CH:20]([N:17]1[CH2:16][CH2:15][CH:14]([O:13][CH3:12])[CH2:19][CH2:18]1)[C:23]1[CH:24]=[N:25][C:26]([CH3:29])=[N:27][CH:28]=1)=[O:6]Participants
3
Procedure
From 2,3-dichlorobenzoic acid and 2-(4-methoxypiperidin-1-yl)-2-(2-methylpyrimidin-5-yl)ethanamine.
Sources & evidence
- ORD record
- ord-5ec86c673a4e45018161315c702d02f5
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09415055B2
Reaction notes
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