Allyl chloride → HCID 19047282, compound
Reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[O:9][C:10]3[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=3[N:12]=2)[CH2:4][CH2:3]1.[CH2:17]([Cl:20])[CH:18]=[CH2:19]>>[Cl-:20].[CH2:17]([N+:2]1([CH3:1])[CH2:3][CH2:4][N:5]([C:8]2[O:9][C:10]3[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=3[N:12]=2)[CH2:6][CH2:7]1)[CH:18]=[CH2:19]Participants
3
Procedure
Using 435 mg of 2-(4-methyl-1-piperazinyl)benzoxazole and 0.24 ml of allyl chloride, the same treatment of Example 2 was conducted to obtain 504 mg of the title compound.
Sources & evidence
- ORD record
- ord-7fc1a2c9eb9646f083caa2b255d0271c
- Source dataset
- uspto-grants-1997_05
- Patent number
- US05631257
Reaction notes
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