Sodium Acetate → HCID 178446965, compound
Reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[CH:8][C:7]([C:13]#[N:14])=[C:6]2[O:15][CH:16]1[CH2:21][CH2:20]O[CH2:18][CH2:17]1)=O.[CH:22]1([NH:25][C:26]2[S:27][CH2:28][C:29](=[O:31])[N:30]=2)[CH2:24][CH2:23]1.C([O-])(=O)C.[Na+]>C(O)(=O)C>[CH:22]1([NH:25][C:26]2[S:27]/[C:28](=[CH:1]\[C:3]3[CH:4]=[C:5]4[C:10](=[CH:11][CH:12]=3)[N:9]=[CH:8][C:7]([C:13]#[N:14])=[C:6]4[O:15][CH:16]([CH2:17][CH3:18])[CH2:21][CH3:20])/[C:29](=[O:31])[N:30]=2)[CH2:24][CH2:23]1Participants
5
Procedure
Similar procedure as described in example 28c was used, starting from 6-formyl-4-(tetrahydro-pyran-4-yloxy)-quinoline-3-carbonitrile (example 64b), 2-cyclopropylamino-thiazol-4-one (example 37c), sodium acetate and acetic acid to give 6-[2-cyclopropylamino-4-oxo-4H-thiazol-(5Z)-ylidenemethyl]-4-(1-ethyl-propoxy)-quinoline-3-carbonitrile. LC-MS m/e 407 (MH+).
Sources & evidence
- ORD record
- ord-b16fcc5aa7434109bb12fb9dc8b1750c
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07250515B2
Reaction notes
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