2,3-Dichlorobenzoic acid → HCID 86716296, 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.[CH:12]1([CH2:15][CH:16]([C:19]2[C:20]([CH3:26])=[N:21][C:22]([CH3:25])=[CH:23][CH:24]=2)[CH2:17][NH2:18])[CH2:14][CH2:13]1>>[Cl:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH:18][CH2:17][CH:16]([C:19]1[C:20]([CH3:26])=[N:21][C:22]([CH3:25])=[CH:23][CH:24]=1)[CH2:15][CH:12]1[CH2:13][CH2:14]1)=[O:6]Participants
3
Procedure
From 2,3-dichlorobenzoic acid and 3-cyclopropyl-2-(2,6-dimethyl-pyridin-3-yl)-propylamine. LCMS (MH+): m/z=377.1, tR (minutes, Method G)=1.68
Sources & evidence
- ORD record
- ord-67dfa52b740a427d9ba2cdf974c7bd4c
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102591B2
Reaction notes
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