Hydrochloric Acid → Rivaroxaban

HRID 1054158Notes

Reaction equation

HRID 1054158 reaction equation
[Cl:1][C:2]1[S:6][C:5]([C:7]([N:9](C=O)[CH2:10][C@@H:11]2[O:15][C:14](=[O:16])[N:13]([C:17]3[CH:22]=[CH:21][C:20]([N:23]4[CH2:28][CH2:27][O:26][CH2:25][C:24]4=[O:29])=[CH:19][CH:18]=3)[CH2:12]2)=[O:8])=[CH:4][CH:3]=1.ClCCl.Cl>CO>[CH:19]1[C:20]([N:23]2[C:24](=[O:29])[CH2:25][O:26][CH2:27][CH2:28]2)=[CH:21][CH:22]=[C:17]([N:13]2[C:14](=[O:16])[O:15][C@@H:11]([CH2:10][NH:9][C:7]([C:5]3[S:6][C:2]([Cl:1])=[CH:3][CH:4]=3)=[O:8])[CH2:12]2)[CH:18]=1

Participants

5

Procedure

In four neck round bottom flask charge 5-chloro-N-formyl-N-({(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl}methyl)thiophene-2-carboxamide (120 g), dichloromethane (2400 ml) and hydrochloric acid OR sulphuric acid (120 ml) at 25-30° C. Obtained reaction mixture is heated to reflux for 4 to 5 h. After completion of reaction, concentrate reaction mass under reduced pressure to obtain residue. Added Dichloromethane (120 ml) and slowly added Methanol (600 ml) to the residue. The precipitated solid is filtered off and washed by methanol (240 ml)

Workup

  1. customObtained
  2. customreaction mixture
  3. temperatureis heated
  4. temperatureto reflux for 4 to 5 h
  5. customAfter completion of reaction
  6. concentrationconcentrate
  7. customreaction mass under reduced pressure
  8. customto obtain residue
  9. filtrationThe precipitated solid is filtered off
  10. washwashed by methanol (240 ml)

Sources & evidence

ORD record
ord-44be849f3a6c47439e2a85eca12a77a9
Source dataset
uspto-grants-2016_07
Patent number
US09394292B2

Reaction notes

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