Diisopropylethylamine → HCID 178434021, compound
Reaction equation
CS[C:3]1[S:4]/[C:5](=[CH:9]\[C:10]2[CH:11]=[C:12]3[C:17](=[CH:18][CH:19]=2)[N:16]=[CH:15][CH:14]=[CH:13]3)/[C:6](=[O:8])[N:7]=1.[CH3:20][N:21]1[C:25]([CH3:26])=[C:24]([CH2:27][NH2:28])[C:23]([CH3:29])=[N:22]1.CCN(C(C)C)C(C)C>>[CH3:20][N:21]1[C:25]([CH3:26])=[C:24]([CH2:27][NH:28][C:3]2[S:4]/[C:5](=[CH:9]\[C:10]3[CH:11]=[C:12]4[C:17](=[CH:18][CH:19]=3)[N:16]=[CH:15][CH:14]=[CH:13]4)/[C:6](=[O:8])[N:7]=2)[C:23]([CH3:29])=[N:22]1Participants
4
Procedure
Similar procedure as described in example 1b was used, starting from 2-methylsulfanyl-5-[1-quinolin-6-yl-meth-(Z)-ylidene]-thiazol-4-one, (1,3,5-trimethyl-1H-pyrazol-4-ylmethyl)-amine and DIEA to give 2-[(1,3,5-trimethyl-1H-pyrazol-4-ylmethyl)-amino]-5-[1-quinolin-6-yl-meth-(Z)-ylidene]-thiazol-4-one. LC-MS m/e 378 (MH+).
Sources & evidence
- ORD record
- ord-5a38dbc79fc048d1afde991e8912d6ad
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07326786B2
Reaction notes
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