N,N,N',N'-Tetramethylmethanediamine → HCID 19042887, compound

HRID 1683283Notes

Reaction equation

HRID 1683283 reaction equation
CN([CH2:4][N:5]([CH3:7])[CH3:6])C.C(Cl)(=O)C.[CH3:12][O:13][C:14]1[CH:29]=[CH:28][C:17]([O:18][C:19]2[CH:20]=[C:21]3[C:25](=[CH:26][CH:27]=2)[NH:24][CH:23]=[CH:22]3)=[CH:16][CH:15]=1>C(Cl)Cl>[CH3:7][N:5]([CH2:4][C:22]1[C:21]2[C:25](=[CH:26][CH:27]=[C:19]([O:18][C:17]3[CH:28]=[CH:29][C:14]([O:13][CH3:12])=[CH:15][CH:16]=3)[CH:20]=2)[NH:24][CH:23]=1)[CH3:6]

Participants

5

Reactant 3

HCID 5829N,N,N',N'-TetramethylmethanediamineHCID 6367Acetyl chlorideHCID 19042832HCID 19042832, compound

Product 1

HCID 19042887HCID 19042887, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

N,N,N',N'-Tetramethyldiaminomethane (0.29 g, 0.39 mL, 2.82 mmol) was dissolved in CH2Cl2 (dry; 8.5 mL) and the stirred solution cooled in an ice-bath. Acetyl chloride (0.23 g, 0.21 mL, 2.95 mmol) was added dropwise (syringe) over 10 min, to give a white suspension. After stirring for a further 20 min. with cooling maintained, a solution of 5-(4-methoxyphenoxy)indole (0.5 g, 2.09 mmol) in CH2Cl2 (7.2 mL) was added dropwise, over 20 min. The cooling was removed and the resulting clear solution was stirred for 1 hr at room temperature. The solution was then diluted with CH2Cl2, washed with 10% aq. NaOH (2×) followed by saturated aqueous NACl and dried (MgSO4). Evaporation in vacuo gave 3-(N,N-dimethylaminomethyl)-5-(4-methoxyphenoxy)indole as a gum. This material was dissolved in DMF (dry; 7 mL) and potassium cyanide (0.52 g, 8.0 mmol) was added, followed by methyl iodide (1.19 g, 0.52 mL, 8.35 mmol). The mixture became cloudy and eventually opaque. After stirring at room temperature for 36 hr, water was added and the mixture was extracted with Et2O (2×). The combined organic layers were washed with H2O (2×) and then with saturated aqueous NaCl, dried (MgSO4) and evaporated to give an almost colourless gum. This was triturated with Et2O to give: 3-cyanomethyl-5-(4-methoxyphenoxy)indole as a virtually colourless solid, 0.334 g (57%).

Workup

  1. temperaturethe stirred solution cooled in an ice-bath
  2. customto give a white suspension
  3. temperaturewith cooling
  4. temperaturemaintained
  5. customThe cooling was removed
  6. stirringthe resulting clear solution was stirred for 1 hr at room temperature
  7. additionThe solution was then diluted with CH2Cl2
  8. washwashed with 10% aq. NaOH (2×)
  9. dry with materialdried (MgSO4)
  10. customEvaporation in vacuo

Sources & evidence

ORD record
ord-e6bd6cacbaeb429d91cb22e07f60f1c7
Source dataset
uspto-grants-1997_06
Patent number
US05637593

Reaction notes

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