Sodium Iodide → tert-Butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylate

HRID 1408084Notes

Reaction equation

HRID 1408084 reaction equation
Cl[CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][N:7]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:6][CH2:5]1.[Na+].[I-].[CH3:19][NH2:20]>>[CH3:19][NH:20][CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][N:7]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:6][CH2:5]1

Participants

4

Conditions

Temperature
70 °C

Procedure

Into a 50-mL sealed tube, was placed tert-butyl 4-(2-chloroethyl)piperazine-1-carboxylate (300 mg, 1.21 mmol, 1.00 equiv), methylamine (in ethanol) (10 mL), and NaI (100 mg). The resulting solution was stirred for 12 h at 70° C. in an oil bath. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 3 mL of water and adjusted to pH 7-8 with sodium bicarbonate (5%). The resulting solution was extracted with 2×5 mL of dichloromethane and the organic layers combined. The resulting mixture was washed with 1×3 mL of water and 1×3 mL of brine. The resulting mixture was concentrated under vacuum. This resulted in 180 mg (crude) of tert-butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylate as brown oil.

Workup

  1. customInto a 50-mL sealed tube
  2. concentrationThe resulting mixture was concentrated under vacuum
  3. additionThe resulting solution was diluted with 3 mL of water
  4. extractionThe resulting solution was extracted with 2×5 mL of dichloromethane
  5. washThe resulting mixture was washed with 1×3 mL of water and 1×3 mL of brine
  6. concentrationThe resulting mixture was concentrated under vacuum
  7. customThis resulted in 180 mg (crude) of tert-butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylate as brown oil

Sources & evidence

ORD record
ord-8e61929c6fe24f4f8b15c2ae52ae2cde
Source dataset
uspto-grants-2014_12
Patent number
US08916569B2

Reaction notes

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