HCID 10536778, compound → HCID 23132418, compound
Reaction equation
C(O[C:4]1[C:5](=[O:16])[C:6](=[O:15])[C:7]=1[NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)C.[Cl:17][C:18]1[CH:31]=[CH:30][C:21]([O:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][NH2:29])=[CH:20][CH:19]=1>>[Cl:17][C:18]1[CH:31]=[CH:30][C:21]([O:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][NH:29][C:4]2[C:5](=[O:16])[C:6](=[O:15])[C:7]=2[NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=2)=[CH:20][CH:19]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in example 1B starting from 3-ethoxy-4-(pyridin-2-yl-amino)-3-cyclobutene-1,2-dione and 6-(4-chlorophenoxy)-hexylamine.
Sources & evidence
- ORD record
- ord-c51aeca4f0d245a189e72f78e490679d
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08450348B2
Reaction notes
Loading…