Sodium Carbonate → HCID 19776771, compound
Reaction equation
Cl.[S:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[CH:7]([C:28]1[CH:32]=[CH:31][S:30][CH:29]=1)[O:8][CH:9]1[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][CH2:17][O:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=2[N+:25]([O-:27])=[O:26])[CH2:11][CH2:10]1.C(=O)([O-])[O-].[Na+].[Na+]>>[S:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[CH:7]([C:28]1[CH:32]=[CH:31][S:30][CH:29]=1)[O:8][CH:9]1[CH2:10][CH2:11][N:12]([CH2:15][CH2:16][CH2:17][O:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=2[N+:25]([O-:27])=[O:26])[CH2:13][CH2:14]1Participants
3
Procedure
The hydrochloride obtained in the above was treated with 5% aqueous sodium carbonate to give oily 4-[(2-thienyl)-3-thienylmethoxy]-1-[3-(2-nitrophenoxy)propyl]piperidine.
Sources & evidence
- ORD record
- ord-70a7b143575346ffb39e1d5bf6745ddf
- Source dataset
- uspto-grants-1993_03
- Patent number
- US05190959
Reaction notes
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