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5-Bromo-2-chloro-N-methoxy-N-methylnicotinamide → 1-(5-Bromo-2-chloropyridin-3-yl)ethanone

HRID 643974
Notes
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Reaction equation

HRID 643974 reaction equation
[Br:1][C:2]1[CH:3]=[N:4][C:5]([Cl:14])=[C:6]([CH:13]=1)[C:7](N(OC)C)=[O:8].[CH3:15][Mg]Br>C1COCC1>[Br:1][C:2]1[CH:13]=[C:6]([C:7](=[O:8])[CH3:15])[C:5]([Cl:14])=[N:4][CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 568289985-Bromo-2-chloro-N-methoxy-N-methylnicotinamideHCID 178418573HCID 178418573, compound

Product 1

HCID 254178651-(5-Bromo-2-chloropyridin-3-yl)ethanone

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-78 °C

Procedure

Starting material 5-bromo-2-chloro-N-methoxy-N-methylnicotinamide (5.0 g, 17.89 mmol) was charged into a 250 ml round bottom flask and the flask was chilled to −78° C. Methyl magnesium bromide 96.5 ml, 19.68 mmol) in 5 ml THF was added dropwise via addition funnel. The resulting mixture was allowed to stir for 3 hours at −78° C. After removing the THF solvent via rotatory evaporation under reduced pressure, the reaction mixture was partitioned between ethylacetate and saturated aqueous sodium bicarbonate. After removing the ethylacetate, the resulting crude product was subject to a silica gel column with 20% ethylacetate in hexane. The resulting product (2.28 g, y=54.3%) was used for the following step.

Workup

  1. additionwas charged into a 250 ml round bottom flask
  2. customAfter removing the THF solvent
  3. customvia rotatory evaporation under reduced pressure
  4. customthe reaction mixture was partitioned between ethylacetate and saturated aqueous sodium bicarbonate
  5. customAfter removing the ethylacetate

Sources & evidence

ORD record
ord-2248edbebf3d43fdafeab039658ef756
Source dataset
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07700636B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes