Sodium Hydroxide → Rotigotine

HRID 886655Notes

Reaction equation

HRID 886655 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>[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

5

Procedure

150 g Rotigotine hydrochloride were added to a solution of 17.05 g NaOH in 218 g ethanol (96%). The resulting mixture was stirred for approximately 10 minutes. Then 23.7 g of sodium phosphate buffer solution (8.35 g Na2HPO4×2H2O and 16.07 g NaH2PO4×2H2O in 90.3 g water) was added. Insoluble or precipitated solids were separated from the mixture by filtration. The filter was rinsed with 60.4 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 60.4 g ethanol (96%)

Sources & evidence

ORD record
ord-5ce2dfb4faf6479cbf5f28b8b3ca2af1
Source dataset
uspto-grants-2012_08
Patent number
US08246979B2

Reaction notes

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