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Potassium Iodide → 2-(Ethylamino)-4,5-dimethylthiophene-3-carbonitrile

HRID 471489
Notes
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Reaction equation

HRID 471489 reaction equation
[CH2:1]([NH:8][C:9]1[S:10][C:11]([CH3:17])=[C:12]([CH3:16])[C:13]=1[C:14]#[N:15])[C:2]1C=CC=CC=1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+].C(I)C>C(#N)C.C(OCC)(=O)C>[CH2:1]([NH:8][C:9]1[S:10][C:11]([CH3:17])=[C:12]([CH3:16])[C:13]=1[C:14]#[N:15])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 4875Potassium IodideHCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 3194512-(Benzylamino)-4,5-dimethylthiophene-3-carbonitrile

Product 1

HCID 574569162-(Ethylamino)-4,5-dimethylthiophene-3-carbonitrile

Reagents, catalysts & solvents 2

HCID 6342
Acetonitrile
Solvent
HCID 8857Ethyl AcetateSolvent

Procedure

To a mixture of 2-(benzylamino)-4,5-dimethylthiophene-3-carbonitrile (302 mg, 10 mmol), potassium carbonate (276 mg, 2.0 mmol), and a catalytic amount of potassium iodide in acetonitrile (1 mL) in a 20 mL microwave vial was added ethyl iodide (310 mg, 2.0 mmol). The reaction vial was placed in a microwave reactor for 15 minutes at 165° C. The reaction mixture was dissolved in ethyl acetate and washed with water and brine. The ethyl acetate portion was dried over sodium sulfate and solvent was evaporated under reduced pressure, and the product was purified by prep HPLC using acetonitrile/water as solvent. MS 181 (MH+).

Workup

  1. customThe reaction
  2. washwashed with water and brine
  3. dry with materialThe ethyl acetate portion was dried over sodium sulfate and solvent
  4. customwas evaporated under reduced pressure
  5. customthe product was purified by prep HPLC

Sources & evidence

ORD record
ord-a93d6458f15041ed81a5a9914e88ee73
Source dataset
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08633186B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes