Reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[CH:9][C:4]=1[CH:5]=[CH:6][CH2:7]O.S(Cl)(Cl)=O.[NH:17]1[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1>>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[CH:9][C:4]=1/[CH:5]=[CH:6]/[CH2:7][N:17]1[CH2:22][CH2:21][N:20]([CH2:7]/[CH:6]=[CH:5]/[C:4]2[CH:9]=[CH:10][CH:11]=[CH:12][C:3]=2[O:2][CH3:1])[CH2:19][CH2:18]1Participants
4
Procedure
2-Methoxy-cinnamylalcohol (1.44 g) was chlorinated using thionylchloride. Subsequently, reaction with piperazine and other treatments were performed as described in Preparation Example 2, to thereby obtain 314 mg of a salt as colorless prisms.
Workup
- customas described in Preparation Example 2
Sources & evidence
- ORD record
- ord-d2aea31453084c8dba037f866c0833b5
- Source dataset
- uspto-grants-1998_03
- Patent number
- US05723465
Linked notes
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