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3-Methoxypropylamine → HCID 57625429, compound

HRID 331191
Notes
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Reaction equation

HRID 331191 reaction equation
Cl[C:2]1[N:7]=[CH:6][C:5]([S:8]([NH2:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH3:12][O:13][CH2:14][CH2:15][CH2:16][NH2:17]>>[CH3:12][O:13][CH2:14][CH2:15][CH2:16][NH:17][C:2]1[N:7]=[CH:6][C:5]([S:8]([NH2:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 16723-MethoxypropylamineHCID 12015126-chloropyridine-3-sulfonamide

Product 1

HCID 57625429HCID 57625429, compoundYield 78%

Conditions

Temperature
100 °C

Procedure

A mixture of 6-chloropyridine-3-sulfonamide (5 g, 0.025 mol) and 3-methoxy propylamine (50 ml) is stirred at 100° C. for 12 h. The mixture is cooled and excess reagent is removed by distillation. The residue is suspended in DCM (25 ml) and cooled. The precipitate is filtered, washed with cold ammonium hydroxide (2×50 ml) and dried under vacuum to afford 5 g (78%) of the titled compound as a white solid. mp: 129-132° C., LC/MS: (ES+) 246.

Workup

  1. temperature
The mixture is cooled
  • customexcess reagent is removed by distillation
  • temperaturecooled
  • filtrationThe precipitate is filtered
  • washwashed with cold ammonium hydroxide (2×50 ml)
  • customdried under vacuum
  • Sources & evidence

    ORD record
    ord-73a9e1dce66240e7ae895d8f06b89d00
    Source dataset
    uspto-grants-2014_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08877757B2

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes