3-Chloro-2-methyl-1-propene → HCID 23369594, compound
Reaction equation
[CH2:1]([C:3]1[C:4](=[O:15])[NH:5][C:6]2[C:11]([CH:12]=1)=[C:10]([OH:13])[CH:9]=[CH:8][C:7]=2[CH3:14])[CH3:2].Cl[CH2:17][C:18]([CH3:20])=[CH2:19]>C(Cl)(Cl)Cl.CCCCCC>[CH2:1]([C:3]1[C:4](=[O:15])[NH:5][C:6]2[C:11]([CH:12]=1)=[C:10]([O:13][CH2:19][C:18]([CH3:20])=[CH2:17])[CH:9]=[CH:8][C:7]=2[CH3:14])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Using 3-ethyl-5-hydroxy-8-methylcarbostyril (0.91 g, 4.87 mmol) and 3-chloro-2-methyl-1-propene (0.485 g, 5.36 mmol), the procedure of Reference Example 31 was followed (reaction, post-treatment, and recrystallization from chloroform-n-hexane) to obtain 0.94 g of the title compound as pale brown crystals (75.1%).
Sources & evidence
- ORD record
- ord-e77bf4913191497aaa917c83096cbbd7
- Source dataset
- uspto-grants-1996_11
- Patent number
- US05576324
Reaction notes
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