Thiochroman-4-one → HCID 24991559, compound
Reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[CH3:15][C:16]1[O:20][C:19]([CH2:21][NH2:22])=[CH:18][CH:17]=1.[S:23]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[C:26](=O)[CH2:25][CH2:24]1>>[CH3:15][C:16]1[O:20][C:19]([CH2:21][NH:22][C:8]2[CH:7]=[CH:6][C:5]3[C:4]([NH:1][CH:26]4[C:27]5[C:32](=[CH:31][CH:30]=[CH:29][CH:28]=5)[S:23][CH2:24][CH2:25]4)=[CH:13][CH:12]=[CH:11][C:10]=3[N:9]=2)=[CH:18][CH:17]=1Participants
4
Procedure
The title compound, MS: m/e=402.5 (M+H+), was prepared from 5-nitro-2-chloroquinoline, 5-methyl-2-furanmethanamine and thiochroman-4-one as described in example 26.
Sources & evidence
- ORD record
- ord-7baeebd5724a43f08a363aeb9a5965aa
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825253B2
Reaction notes
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