2,3-Dichlorobenzoic acid → HCID 86716301, 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([C:15]2[N:20]=[CH:19][C:18]([CH:21]([CH2:24][C:25]3([C:28]([F:31])([F:30])[F:29])[CH2:27][CH2:26]3)[CH2:22][NH2:23])=[CH:17][CH:16]=2)[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:23][CH2:22][CH:21]([C:18]1[CH:19]=[N:20][C:15]([CH:12]2[CH2:13][CH2:14]2)=[CH:16][CH:17]=1)[CH2:24][C:25]1([C:28]([F:29])([F:30])[F:31])[CH2:27][CH2:26]1)=[O:6]Participants
3
Procedure
From 2,3-dichlorobenzoic acid and 2-(6-cyclopropyl-pyridin-3-yl)-3-(1-trifluoromethyl-cyclopropyl)-propylamine. LCMS (MH+): m/z=457.1, tR (minutes, Method G)=1.96
Sources & evidence
- ORD record
- ord-0ea07f164a7c4658a6028c13ea7c690a
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102591B2
Reaction notes
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