Hydrochloric Acid → 2-Methylthieno[2,3-c]pyridine

HRID 254437Notes

Reaction equation

HRID 254437 reaction equation
CO[CH:3](OC)[CH2:4][N:5]([CH2:16][C:17]1[S:18][C:19]([CH3:22])=[CH:20][CH:21]=1)S(C1C=CC(C)=CC=1)(=O)=O.Cl.[OH-].[Na+].O.C([O-])(O)=O.[Na+]>O1CCOCC1.CCOCC>[CH3:22][C:19]1[S:18][C:17]2=[CH:16][N:5]=[CH:4][CH:3]=[C:21]2[CH:20]=1

Participants

7

Conditions

Temperature
107.5 °C

Procedure

76059-85: N-(2,2-Dimethoxy-ethyl)4-methyl-N-(5-methyl-thiophen-2-ylmethyl)-benzenesulfonamide (2) (50.56 g crude) was dissolved in dioxane (250 mL) and conc. HCl (200 mL) was added cautiously. The dark red solution was heated at gentle reflux (105 to 110° C.) for 24 hours. The volume was reduced by approximately half, then diluted with ether (200 mL). The pH was adjusted to between 7 and 8 using 50% NaOH/H2O and sat NaHCO3 solution with cooling. More ether (400 mL) was added, the mixture was filtered to remove insoluble material and the phases separated. The organic phase was washed with water (2×350 mL), dried (MgSO4) and condensed to dark red-brown oil. Purification was accomplished using Kugelrohr distillation (120 to 130° C.) to give 11.89 g of title compound as a pale yellow liquid.

Workup

  1. temperatureThe dark red solution was heated
  2. temperaturewith cooling
  3. filtrationthe mixture was filtered
  4. customto remove insoluble material
  5. customthe phases separated
  6. washThe organic phase was washed with water (2×350 mL)
  7. customdried
  8. custom(MgSO4) and condensed to dark red-brown oil
  9. customPurification
  10. distillationKugelrohr distillation (120 to 130° C.)

Sources & evidence

ORD record
ord-1175847722df4fae85cc289fd7096087
Source dataset
uspto-grants-2011_01
Patent number
US07875627B2

Reaction notes

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