Acetonitrile → Debrisoquine
Reaction equation
[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][NH:2]1.N[N:12]=[CH:13]S(O)(=O)=O.C(#[N:20])C>>[CH:7]1[CH:8]=[CH:9][C:10]2[CH2:1][N:2]([C:13]([NH2:12])=[NH:20])[CH2:3][CH2:4][C:5]=2[CH:6]=1Participants
4
Procedure
Tetrahydroisoquinoline (0.013 m) is treated with aminoiminomethanesulfonic acid (0.01 m) at ambient temperature. After completion of the reaction, it is diluted with acetonitrile, cooled and the solid product is collected by filtration.
Workup
- customAfter completion of the reaction, it
- temperaturecooled
- filtrationthe solid product is collected by filtration
Sources & evidence
- ORD record
- ord-0cd5d279cd8c49429e14cc8a53a6b393
- Source dataset
- uspto-grants-1987_04
- Patent number
- US04656291
Reaction notes
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