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Triethylamine → HCID 178481146, compound

HRID 1285327
Notes
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Reaction equation

HRID 1285327 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]1
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 102205613-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amineHCID 202489501-Methyl-2-methylthio-imidazolin-4-one hydroiodide

Product 1

HCID 178481146HCID 178481146, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

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
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04567176

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes