9-Anthracenecarboxaldehyde → HCID 86598796, compound
Reaction equation
[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH2:24])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:27])[F:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:29]1[C:42]2[C:33](=[CH:34][C:35]3[C:40]([C:41]=2[CH:43]=O)=[CH:39][CH:38]=[CH:37][CH:36]=3)[CH:32]=[CH:31][CH:30]=1>>[CH:39]1[C:40]2[C:35](=[CH:34][C:33]3[C:42]([C:41]=2[CH2:43][NH:24][C:20]2[CH:21]=[CH:22][CH:23]=[C:18]([C:17]4[C:16]5[C:11](=[C:12]([C:25]([F:28])([F:26])[F:27])[CH:13]=[CH:14][CH:15]=5)[N:10]=[CH:9][C:8]=4[CH2:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)[CH:19]=2)=[CH:29][CH:30]=[CH:31][CH:32]=3)[CH:36]=[CH:37][CH:38]=1Participants
3
Procedure
This compound was prepared according to the procedure of example 66, substituting 3-(3-benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine and anthracene-9-carbaldehyde. MS (ESI) m/z 569.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-59b31b4e593947a599693475b5a74231
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576215B2
Reaction notes
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