Diisopropylethylamine → HCID 178466955, compound
Reaction equation
[CH2:1]([O:3][C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11](/[CH:14]=[C:15]3/[C:16](=[O:22])[N:17]=[C:18](SC)[S:19]/3)[CH:12]=2)[N:7]=[CH:6][C:5]=1[C:23]#[N:24])[CH3:2].[CH3:25][O:26][CH2:27][CH2:28][O:29][CH2:30][CH2:31][NH2:32].CCN(C(C)C)C(C)C>>[CH3:25][O:26][CH2:27][CH2:28][O:29][CH2:30][CH2:31][NH:32][C:18]1[S:19]/[C:15](=[CH:14]\[C:11]2[CH:12]=[C:13]3[C:8](=[CH:9][CH:10]=2)[N:7]=[CH:6][C:5]([C:23]#[N:24])=[C:4]3[O:3][CH2:1][CH3:2])/[C:16](=[O:22])[N:17]=1Participants
4
Procedure
Similar procedure as described in example 14h was used, starting from 4-ethoxy-6-[2-methylsulfanyl-4-oxo-4H-thiazol-(5Z)-ylidenemethyl]-quinoline-3-carbonitrile (example 14g), 2-(2-methoxy-ethoxy)-ethylamine and DIEA to give 6-[2-[2-(2-methoxy-ethoxy)-ethylamino]-4-oxo-4H-thiazol-(5Z)-ylidenemethyl]-4-ethoxy-quinoline-3-carbonitrile. LC-MS m/e 427 (MH+).
Sources & evidence
- ORD record
- ord-342a350a10444c7ba59ef68482c16b75
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07250515B2
Reaction notes
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