Phenylacetylene → 7-Diethylamino-3-(4-phenyl-[1,2,3]triazol-1-yl)-chromen-2-one
Reaction equation
[CH2:1]([N:3]([CH2:18][CH3:19])[C:4]1[CH:13]=[C:12]2[C:7]([CH:8]=[C:9]([N:15]=[N+:16]=[N-:17])[C:10](=[O:14])[O:11]2)=[CH:6][CH:5]=1)[CH3:2].[C:20]1([C:26]#[CH:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[CH2:18]([N:3]([CH2:1][CH3:2])[C:4]1[CH:13]=[C:12]2[C:7]([CH:8]=[C:9]([N:15]3[CH:27]=[C:26]([C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=4)[N:17]=[N:16]3)[C:10](=[O:14])[O:11]2)=[CH:6][CH:5]=1)[CH3:19]Participants
3
Procedure
This example illustrates the fluorogenic conjugation of 7-diethylamino-3-azidocoumarin and phenylacetylene to form 7-diethylamino-3-(4-phenyl-[1,2,3]triazol-1-yl)-chromen-2-one.
Sources & evidence
- ORD record
- ord-5fe75548be3b4eb5a719ebad0f0d6847
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07745229B2
Reaction notes
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