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Toluene → 1-(6-Bromo-pyridin-2-yl)-2-methoxymethoxy-1-methoxymethoxymethyl-ethylamine

HRID 538304
Notes
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Reaction equation

HRID 538304 reaction equation
[Br:1][C:2]1[N:7]=[C:6]([C:8]([CH2:17][O:18][CH2:19][O:20][CH3:21])([CH2:12][O:13][CH2:14][O:15][CH3:16])C(O)=O)[CH:5]=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.C([N:31](CC)CC)C.[OH-].[Na+]>C1COCC1>[Br:1][C:2]1[N:7]=[C:6]([C:8]([NH2:31])([CH2:17][O:18][CH2:19][O:20][CH3:21])[CH2:12][O:13][CH2:14][O:15][CH3:16])[CH:5]=[CH:4][CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 1140TolueneHCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 866680182-(6-Bromo-pyridin-2-yl)-3-methoxymethoxy-2-methoxymethoxymethyl-propionic acid

Product 1

HCID 866680191-(6-Bromo-pyridin-2-yl)-2-methoxymethoxy-1-methoxymethoxymethyl-ethylamine

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent

Conditions

Temperature
100 °C

Procedure

To a suspension of 2-(6-bromo-pyridin-2-yl)-3-methoxymethoxy-2-methoxymethoxymethyl-propionic acid (18.0 g) in toluene (150 ml)diphenyl phosphoryl azide (4.08 g, 148.27 mmol) and triethylamine (14.97 g [20.6 ml], 148.27 mmol) were added at rt and stirred at 100° C. for 15 h. Reaction mixture was cooled to rt and concentrated under reduced pressure. The residue obtained was dissolved in THF (600 ml) and 20% NaOH solution was added at rt and stirred for 1 h. Solvent was removed under reduced pressure and the product formed was extracted with ethyl acetate. Organic layer was washed with brine, followed by dried over MgSO4. The organic portion was concentrated under reduced pressure and column chromatographic purification of the crude product using 35% ethyl acetate in hexane furnished title compound as a brown liquid. Yield=15.0 g (88% [2 steps]). TLC (70% ethyl acetate in hexane) Rf=0.51; LCMS: RtH7=0.28, [M+1]=335.0 and 337.0.

Workup

  1. additionwere added at rt
  2. customReaction mixture
  3. temperaturewas cooled to rt
  4. concentrationconcentrated under reduced pressure
  5. customThe residue obtained
  6. stirringstirred for 1 h
  7. customSolvent was removed under reduced pressure
  8. customthe product formed
  9. extractionwas extracted with ethyl acetate
  10. washOrganic layer was washed with brine
  11. dry with materialby dried over MgSO4
  12. concentrationThe organic portion was concentrated under reduced pressure and column chromatographic purification of the crude product

Sources & evidence

ORD record
ord-ec442df059c64201a14f9fdb9fb9ea62
Source dataset
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08865712B2

Reaction notes

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