Dimethylformamide → 2-amino-5-cyano-N-methylbenzamide

HRID 1947938Notes

Reaction equation

HRID 1947938 reaction equation
[NH2:1][C:2]1[CH:11]=[CH:10][C:9](Br)=[CH:8][C:3]=1[C:4]([NH:6][CH3:7])=[O:5].[CH3:13][N:14](C=O)C>[C-]#N.[Zn+2].[C-]#N.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[NH2:1][C:2]1[CH:11]=[CH:10][C:9]([C:13]#[N:14])=[CH:8][C:3]=1[C:4]([NH:6][CH3:7])=[O:5]

Participants

5

Procedure

A mixture of 2-Amino-5-bromo-N-methylbenzamide (100.0 mg, 0.4365 mmol), zinc cyanide (51.26 mg, 0.4365 mmol), Pd(PPh3)4 (75.67 mg, 0.06548 mmol) in DMF (1.5 mL) was flushed with nitrogen and irradiated in a microwave reactor at 150° C. for 5 minutes. The reaction mixture was poured into water and extracted by ethyl acetate. The combined organic layers were washed with water and brine, concentrated in vacuo and purified on an ISCO Combiflash unit to isolate the desired product (37.0 mg, 48% yield).

Workup

  1. customwas flushed with nitrogen
  2. customirradiated in a microwave reactor at 150° C. for 5 minutes
  3. additionThe reaction mixture was poured into water
  4. extractionextracted by ethyl acetate
  5. washThe combined organic layers were washed with water and brine
  6. concentrationconcentrated in vacuo
  7. custompurified on an ISCO Combiflash unit

Sources & evidence

ORD record
ord-8dc56b3240234096827a48a267f0faa0
Source dataset
uspto-grants-2013_03
Patent number
US08399433B2

Reaction notes

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