Water → HCID 86630675, compound
Reaction equation
Cl.[C:2]1([C:8]2[C:9]([C:17]3[CH:22]=[CH:21][C:20]([CH2:23]N4CCC(C5N=C(C6C=CC=CN=6)NN=5)CC4)=[CH:19][CH:18]=3)=[N:10][C:11]3[N:12]([N:14]=[CH:15][CH:16]=3)[CH:13]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br:41]N1C(=O)CCC1=O.[OH2:49]>C(Cl)(Cl)Cl.ClCCl>[Br:41][C:16]1[CH:15]=[N:14][N:12]2[CH:13]=[C:8]([C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[C:9]([C:17]3[CH:22]=[CH:21][C:20]([CH:23]=[O:49])=[CH:19][CH:18]=3)=[N:10][C:11]=12Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
1.0 g 6-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehyde (prepared as described under example 19) and 0.65 g N-bromosuccinimide are refluxed in 30 ml Chloroform for 5 h. This mixture is worked up by diluting with water and extraction with dichloromethane. The organic layers are dried over Na2SO4 and concentrated to yield the crude product, which is suspended in ethyl acetate/petrol ether. The solid desired product is isolated by filtration.
Workup
- dry with materialThe organic layers are dried over Na2SO4
- concentrationconcentrated
- customto yield the crude product, which
Sources & evidence
- ORD record
- ord-fcee1c75b0164b6180eeeceb21748448
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08614218B2
Reaction notes
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