Allyl bromide → HCID 23020483, compound
Reaction equation
[NH2:1][C:2]1[NH:7][C:6](=[O:8])[C:5]([C:9]2[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=2)=[C:4]([C:15]2[O:16][CH:17]=[CH:18][CH:19]=2)[N:3]=1.[CH2:20](Br)[CH:21]=[CH2:22]>>[CH2:22]([N:7]1[C:6](=[O:8])[C:5]([C:9]2[CH:10]=[CH:11][N:12]=[CH:13][CH:14]=2)=[C:4]([C:15]2[O:16][CH:17]=[CH:18][CH:19]=2)[N:3]=[C:2]1[NH2:1])[CH:21]=[CH2:20]Participants
3
Procedure
The title compound was synthesized in a manner similar to that described for Example 3 from 2-amino-6-(2-furyl)-5-(4-pyridyl)-3,4-dihydro-4-pyrimidinone and allyl bromide.
Sources & evidence
- ORD record
- ord-2fba2a114e094a2db96b0c433a18dc89
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07160892B2
Reaction notes
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