10-(2-(Dimethylamino)propyl)-N,N-dimethyl-10H-phenothiazine-2-sulfonamide → Cinanserin
Reaction equation
[CH:1]1[C:6]([CH2:7][CH:8](N)[C:9]([OH:11])=O)=[CH:5][CH:4]=[C:3](Cl)[CH:2]=1.CC(N(C)C)C[N:17]1[C:26]2[CH:27]=[C:28](S(N(C)C)(=O)=O)[CH:29]=[CH:30][C:25]=2[S:24][C:23]2[CH:22]=[CH:21]C=CC1=2.CC1C=CC(S(O)(=O)=O)=CC=1.CC1C=C(C[C:59]([NH:61][CH2:62]C(OC2C=C(OC)C=CC=2)C)=N)C=CC=1>>[CH3:59][N:61]([CH2:21][CH2:22][CH2:23][S:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[NH:17][C:9](/[CH:8]=[CH:7]/[C:6]1[CH:5]=[CH:4][CH:3]=[CH:2][CH:1]=1)=[O:11])[CH3:62]Participants
4
Procedure
fenclonine; fonazine mesilate; xylamidine tosylate.
Sources & evidence
- ORD record
- ord-b2e1e24f36604409bd73f5a1f75ef3a9
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07175854B2
Reaction notes
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