Triethylamine → HCID 178481146, compound
Reaction equation
[N:1]1([CH2:7][C:8]2[CH:9]=[C:10]([CH:16]=[CH:17][CH:18]=2)[O:11][CH2:12][CH2:13][CH2:14][NH2:15])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.I.[CH3:20][N:21]1[CH2:25][C:24](=[O:26])[N:23]=[C:22]1SC.C(N(CC)CC)C>C(O)C>[N:1]1([CH2:7][C:8]2[CH:9]=[C:10]([CH:16]=[CH:17][CH:18]=2)[O:11][CH2:12][CH2:13][CH2:14][NH:15][C:22]2[N:21]([CH3:20])[CH2:25][C:24](=[O:26])[N:23]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
5
Procedure
3-(3-Piperidinomethylphenoxy)propylamine (2.61 g), 1-methyl-2-methylthioimidazolin-4-one hydroiodide (2.85 g) and triethylamine (3.635 g) were refluxed in ethanol (25 ml) for 5 hours.
Sources & evidence
- ORD record
- ord-66dd92b17ebf4854b17f55dcc424c67a
- Source dataset
- uspto-grants-1986_01
- Patent number
- US04567176
Reaction notes
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