Dimethylamine → HCID 18959684, compound
Reaction equation
[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:18])[CH:7]=[C:8]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)[O:9]2)=[CH:4][CH:3]=1.Br[CH2:20][CH2:21][CH2:22][CH2:23]Cl.[CH3:25][NH:26][CH3:27]>>[CH3:25][N:26]([CH3:27])[CH2:20][CH2:21][CH2:22][CH2:23][O:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6](=[O:18])[CH:7]=[C:8]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)[O:9][C:10]=2[CH:11]=1Participants
4
Procedure
The compound was prepared by a method similar to Example 1 from 7-hydroxyflavone, 1-bromo-4-chlorobutane and dimethylamine: mp 95°-96° C.
Sources & evidence
- ORD record
- ord-cce1dfc208164cf79509173ac5c784a6
- Source dataset
- uspto-grants-1994_01
- Patent number
- US05278174
Reaction notes
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