Propylamine → HCID 18383097, compound
Reaction equation
[CH2:1]([NH2:4])[CH2:2][CH3:3].[NH:5]1[C:13]2[C:8](=[CH:9][C:10]([NH:14][C:15]3[C:16]4[S:23][C:22]([C:24]5[CH:31]=[CH:30][C:27]([CH:28]=O)=[CH:26][CH:25]=5)=[CH:21][C:17]=4[N:18]=[CH:19][N:20]=3)=[CH:11][CH:12]=2)[CH:7]=[CH:6]1>>[NH:5]1[C:13]2[C:8](=[CH:9][C:10]([NH:14][C:15]3[C:16]4[S:23][C:22]([C:24]5[CH:31]=[CH:30][C:27]([CH2:28][NH:4][CH2:1][CH2:2][CH3:3])=[CH:26][CH:25]=5)=[CH:21][C:17]=4[N:18]=[CH:19][N:20]=3)=[CH:11][CH:12]=2)[CH:7]=[CH:6]1Participants
3
Procedure
The title compound was prepared from propylamine and 4-(4-(1H-indol-5-ylamino)-thieno[3,2-d]pyrimidin-6-yl]-benzaldehyde by a procedure analogous to example 17. M.P. 190-205° C.; LC-MS: 414 (MH+); HPLC RT: 4.15 minutes.
Sources & evidence
- ORD record
- ord-83edb220f3c6421fb38f1a8b864a33ef
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06492383B1
Reaction notes
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