Ethanolamine → HCID 10342546, compound
Reaction equation
[CH3:1][C:2]1[NH:3][C:4]2[C:9]([CH:10]=1)=[CH:8][C:7]([NH:11][C:12]1[CH:17]=[CH:16][N:15]=[C:14]3[CH:18]=[C:19]([C:21]4[CH:28]=[CH:27][C:24]([CH:25]=O)=[CH:23][CH:22]=4)[S:20][C:13]=13)=[CH:6][CH:5]=2.[OH:29][CH2:30][CH2:31][NH2:32]>>[CH3:1][C:2]1[NH:3][C:4]2[C:9]([CH:10]=1)=[CH:8][C:7]([NH:11][C:12]1[CH:17]=[CH:16][N:15]=[C:14]3[CH:18]=[C:19]([C:21]4[CH:28]=[CH:27][C:24]([CH2:25][NH:32][CH2:31][CH2:30][OH:29])=[CH:23][CH:22]=4)[S:20][C:13]=13)=[CH:6][CH:5]=2Participants
3
Procedure
The title compound was prepared from 4-[7-(2-methyl-1H-Indol-5-ylamino)-thieno[3,2-b]pyridin-2-yl]-benzaldehyde (60 mg, 0.156 mmol) and 2-hydroxyethylamine (57 mg, 0.939 mmol) by a procedure analogous to example 82. RP18-HPLC RT: 4.078 minutes; API MS: 465.0 (M+1).
Sources & evidence
- ORD record
- ord-c829957a42094a259447bd6fb48e5e28
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06492383B1
Reaction notes
Loading…