Sodium Hydroxide → Rotigotine

HRID 886654Notes

Reaction equation

HRID 886654 reaction equation
[CH3:1][CH2:2][CH2:3][N:4]([C@@H:12]1[CH2:17][C:16]2[CH:18]=[CH:19][CH:20]=[C:21]([OH:22])[C:15]=2[CH2:14][CH2:13]1)[CH2:5][CH2:6][C:7]1[S:11][CH:10]=[CH:9][CH:8]=1.Cl.[OH-].[Na+].P([O-])([O-])([O-])=O.[Na+].[Na+].[Na+]>C(O)C.O>[CH3:1][CH2:2][CH2:3][N:4]([C@@H:12]1[CH2:17][C:16]2[CH:18]=[CH:19][CH:20]=[C:21]([OH:22])[C:15]=2[CH2:14][CH2:13]1)[CH2:5][CH2:6][C:7]1[S:11][CH:10]=[CH:9][CH:8]=1

Participants

6

Procedure

2400 g Rotigotine hydrochloride were added to a solution of 272.8 g NaOH in 3488 g ethanol (96%). The resulting mixture was stirred for approximately 10 minutes. Then 379.2 g of sodium phosphate buffer solution (27.6 g Na2HPO4×2H2O) and 53.2 g NaH2PO4×2H2O in 298.5 g water) was added. Insoluble or precipitated solids were separated from the mixture by filtration. The filter was rinsed with 964 g ethanol (96%) to obtain a particle-free ethanolic solution of rotigotine essentially in the form of the free base.

Workup

  1. customInsoluble or precipitated solids
  2. customwere separated from the mixture by filtration
  3. washThe filter was rinsed with 964 g ethanol (96%)

Sources & evidence

ORD record
ord-8324a7f1851b4352a19073d44d3d3d04
Source dataset
uspto-grants-2012_08
Patent number
US08246979B2

Reaction notes

Loading…