HCID 58049711, compound → HCID 58049706, compound
Reaction equation
[C:1]1([C:7]2[NH:8][C:9]3[C:10]4[N:58]=[C:57]([C:59]5[CH:64]=[CH:63][CH:62]=[CH:61][CH:60]=5)[CH:56]=[C:55]([C:65]5[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=5)[C:11]=4[CH2:12][CH2:13][C:14]=3[CH:15]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([CH:23]4[C:32]5[CH2:31][CH2:30][C:29]6[C:33]([C:43]7[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=7)=[CH:34][C:35]([C:37]7[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=7)=[N:36][C:28]=6[C:27]=5[NH:26][C:25]([C:49]5[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=5)=[N:24]4)[CH:18]=3)[N:16]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>[Pd].C(O)COCCO>[C:49]1([C:25]2[N:24]=[C:23]([C:19]3[CH:20]=[CH:21][CH:22]=[C:17]([C:15]4[C:14]5[C:9](=[C:10]6[N:58]=[C:57]([C:59]7[CH:64]=[CH:63][CH:62]=[CH:61][CH:60]=7)[CH:56]=[C:55]([C:65]7[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=7)[C:11]6=[CH:12][CH:13]=5)[N:8]=[C:7]([C:1]5[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=5)[N:16]=4)[CH:18]=3)[C:32]3[C:27](=[C:28]4[N:36]=[C:35]([C:37]5[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=5)[CH:34]=[C:33]([C:43]5[CH:44]=[CH:45][CH:46]=[CH:47][CH:48]=5)[C:29]4=[CH:30][CH:31]=3)[N:26]=2)[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A suspension of 1,3-bis(2,7,9-triphenyl-1,4,5,6-tetrahydropyrido[3,2-h]quinazolin-4-yl)benzene (5) (4.4 mmol) in 220 diethyleneglycol was heated until total dissolution. 1.2 g Pd/C was then slowly added, and the reaction was refluxed for 6 hours with argon bubbling directly in the solution. The reaction was then stopped, and the suspension cooled to room temperature.
Workup
- temperaturewas heated until total dissolution
- temperaturethe reaction was refluxed for 6 hours with argon bubbling directly in the solution
Sources & evidence
- ORD record
- ord-4352c6a372534f1d85c587f7a1676115
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08475686B2
Reaction notes
Loading…