2-(5-(3-(ethylsulfonyl)phenyl)-3-methyl-9H-pyrido[2,3-b]indol-8-yloxy)ethanol → 2-(3-chloro-5-(3-(ethylsulfonyl)phenyl)-9H-pyrido[2,3-b]indol-8-yloxy)ethanol
Reaction equation
[Cl:1][C:2]1[CH:26]=[N:25][C:5]2[NH:6][C:7]3[C:12]([C:4]=2[CH:3]=1)=[C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([S:19]([CH2:22][CH3:23])(=[O:21])=[O:20])[CH:14]=1)[CH:10]=[CH:9][C:8]=3[OH:24].C(S(C1C=C(C2C=C[C:44]([O:47]CCO)=[C:43]3C=2C2C=C(C)C=NC=2N3)C=CC=1)(=O)=O)C>>[Cl:1][C:2]1[CH:26]=[N:25][C:5]2[NH:6][C:7]3[C:12]([C:4]=2[CH:3]=1)=[C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([S:19]([CH2:22][CH3:23])(=[O:21])=[O:20])[CH:14]=1)[CH:10]=[CH:9][C:8]=3[O:24][CH2:43][CH2:44][OH:47]Participants
3
Procedure
The title compound was prepared from Compound 218 by using an analogous procedure to that outlined in the preparation of Compound 215. 1H NMR (400 MHz, Methanol-d4) δ 8.39 (s, 1 H) 8.14 (m, 1 H) 8.06 (m, 1 H) 8.00 (m, 1 H) 7.87 (t, J=8.0 Hz, 1 H) 7.71 (d, J=4.0 Hz, 1 H) 7.21 (d, J=8.0 Hz, 1 H) 7.16 (d, J=8.0 Hz, 1 H) 4.36 (t, J=4 Hz, 2 H) 4.07 (t, J=4 Hz, 2 H) 3.30 (q, J=7.5 Hz, 2 H) 1.31 (t, J=7.5 Hz, 3 H). [M+H] calc'd for C21H20ClN2O4S, 431; found, 431.
Sources & evidence
- ORD record
- ord-3edd7c417c794a96a88dede590f0e0f3
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08119655B2
Reaction notes
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