N-(2-Aminoethyl)piperidine → HCID 71082809, compound

HRID 1921407Notes

Reaction equation

HRID 1921407 reaction equation
[CH2:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[O:15][C:14]([S:16]([Cl:19])(=[O:18])=[O:17])=[CH:13][CH:12]=2)[CH:4]=1)[CH3:2].[N:20]1([CH2:26][CH2:27][NH2:28])[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1>>[ClH:19].[N:20]1([CH2:26][CH2:27][NH:28][S:16]([C:14]2[O:15][C:11]([C:5]3[CH:4]=[C:3]([CH2:1][CH3:2])[C:8](=[O:9])[NH:7][C:6]=3[CH3:10])=[CH:12][CH:13]=2)(=[O:18])=[O:17])[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1

Participants

3

Reactant 2

HCID 33944N-(2-Aminoethyl)piperidineHCID 86610360HCID 86610360, compound

Product 1

HCID 71082809HCID 71082809, compoundYield 84%

Procedure

5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)furan-2-sulfonyl chloride is reacted with (2-piperidin-1-yl)ethylamine as described in Steps 5 and 6, Example 24 to give the title compound as a solid (84% yield). LC/MS: RT 2.02 min; m/e 394 (M+H).

Sources & evidence

ORD record
ord-ea092a0c5bb94c55aca1c6d83aad2ac7
Source dataset
uspto-grants-2012_05
Patent number
US08173682B2

Reaction notes

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