1-Bromo-2-butanone → HCID 86703032, compound
Reaction equation
[CH:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:14]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:13][N:12]3[CH:21]=[C:22](C(OCC)=O)[N:23]=[C:11]3[N:10]=2)=[CH:5][CH:4]=1)=[O:2].Br[CH2:30][C:31](=O)CC>>[CH2:30]([C:22]1[N:23]=[C:11]2[N:10]=[C:9]([C:6]3[CH:7]=[CH:8][C:3]([CH:1]=[O:2])=[CH:4][CH:5]=3)[C:14]([C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=3)=[CH:13][N:12]2[CH:21]=1)[CH3:31]Participants
3
Procedure
This compound was prepared in a manner according to ethyl 7-(4-formylphenyl)-6-phenylimidazo[1,2-a]pyrimidine-2-carboxylate by using 1-bromobutan-2-one instead of ethyl 3-bromo-2-oxopropanoate in step 5.
Workup
- customThis compound was prepared in a manner
Sources & evidence
- ORD record
- ord-fd6693524dad4383a1ca6b17eb0cdc59
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957064B2
Reaction notes
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