Cyclopropylamine → HCID 9822910, compound
Reaction equation
[CH:1]1([NH2:4])[CH2:3][CH2:2]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]([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>>[CH:1]1([NH:4][CH2:28][C:27]2[CH:26]=[CH:25][C:24]([C:22]3[S:23][C:16]4[C:15]([NH:14][C:10]5[CH:9]=[C:8]6[C:13](=[CH:12][CH:11]=5)[NH:5][CH:6]=[CH:7]6)=[N:20][CH:19]=[N:18][C:17]=4[CH:21]=3)=[CH:31][CH:30]=2)[CH2:3][CH2:2]1Participants
3
Procedure
The title compound was prepared from cyclopropylamine and 4-[4-(1H-indol-5-ylamino)-thieno[3,2-d]pyrimidin-6-yl]-benzaldehyde by a procedure analogous to example 17. M.P. 176-180° C.; LC-MS: 412 (MH+); HPLC RT: 4.10 minutes.
Sources & evidence
- ORD record
- ord-31140d6fcf69453481c459ccef8be0ee
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06492383B1
Reaction notes
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