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Dimethylformamide → HCID 68286493, compound

HRID 1518707
Notes
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Reaction equation

HRID 1518707 reaction equation
NC1[C:3]([Br:13])=[C:4]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[S:5][C:6]=1[Br:7].[H-].[Na+].IC.[CH3:18][N:19]([CH:21]=O)[CH3:20]>>[Br:13][C:3]1[C:21]([N:19]([CH3:18])[CH3:20])=[C:6]([Br:7])[S:5][C:4]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 68285441HCID 68285441, compound2×

Product 1

HCID 68286493HCID 68286493, compoundYield 58.97%

Conditions

Temperature
-5 °C

Procedure

To a solution of Ethyl 4-amino-3,5-dibromothiophene-2-carboxylate (compound 34b, 5.0 g, 15.19 mmol) in DMF (25 ml) was added NaH (60% suspension in mineral oil) (1.82 g, 45.49 mmol) in portion wise manner at a temperature of about −5° C. The reaction mixture was then stirred at −5° C. for 20 min. To the reaction mixture was then added iodomethane (6.47 g, 2.83 ml, 45.59 mmol) and stirring was continued for 40 min at −5° C. The progress of the reaction was monitored by TLC. The reaction mixture was then quenched by addition of cold water (50 ml). the mixture so obtained was then extracted with ethyl acetate (3×100 ml). The combined organic layer was then dried over sodium sulphate and concentrated under reduced pressure to obtain a crude product, which was then purified by flash column chromatography using 2.5% ethyl acetate in hexanes as an eluent to obtain the title compound (3.2 g, 58.97%).

Workup

  1. waitwas continued for 40 min at −5° C
  2. customThe reaction mixture was then quenched by addition of cold water (50 ml)
  3. customthe mixture so obtained
  4. extractionwas then extracted with ethyl acetate (3×100 ml)
  5. dry with materialThe combined organic layer was then dried over sodium sulphate
  6. concentrationconcentrated under reduced pressure
  7. customto obtain a crude product, which
  8. customwas then purified by flash column chromatography

Sources & evidence

ORD record
ord-b2063eb6a2dd48c699f1495af6b4523c
Source dataset
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09072731B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes