Hydrochloric Acid → 5-Methyl-(1,3)oxazolo(4,5-b)pyridine-2-thiol

HRID 549681Notes

Reaction equation

HRID 549681 reaction equation
C([O-])=O.[NH4+].[N+:5]([C:8]1[C:13]([OH:14])=[CH:12][CH:11]=[C:10]([CH3:15])[N:9]=1)([O-])=O.[OH-].[K+].Cl.[C:19](=S)=[S:20]>CCO.[OH-].[OH-].[Pd+2]>[CH3:15][C:10]1[N:9]=[C:8]2[NH:5][C:19](=[S:20])[O:14][C:13]2=[CH:12][CH:11]=1

Participants

8

Conditions

Temperature
70 °C

Procedure

Ammonium formate (1.64 g, 26 mmol) was added to a suspension of Pd(OH)2 on carbon (˜20% Pd, 0.73 g, 1.0 mmol) and 2-nitro-3-hydroxy-6-methylpyridine (2.0 g, 13 mmol) in EtOH (20 mL). The reaction mixture was heated to 70° C. for 1 h at which point the reaction mixture was allowed to cool to rt and was filtered through Celite®. The filtrate was concentrated under reduced pressure, yielding a thick orangish oil. The material was dissolved in EtOH (25 mL) and potassium hydroxide (0.875 g, 15.6 mmol) and carbon disulfide (15 mL) were added. The reaction mixture was heated to reflux overnight. Upon cooling to rt, the reaction mixture was acidified with 1 N HCl, and the resulting solid was collected by filtration. The solid was washed with water (2×) and air dried followed by drying in a 35° C. vacuum oven. LC-MS: RT=5.58 min, [M+H]+=167.0.

Workup

  1. temperatureto cool to rt
  2. filtrationwas filtered through Celite®
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. customyielding a thick orangish oil
  5. temperatureThe reaction mixture was heated
  6. temperatureto reflux overnight
  7. temperatureUpon cooling to rt
  8. filtrationthe resulting solid was collected by filtration
  9. washThe solid was washed with water (2×) and air
  10. customdried
  11. customby drying in a 35° C. vacuum oven

Sources & evidence

ORD record
ord-a62667c51cc741e298f940b160451c66
Source dataset
uspto-grants-2011_05
Patent number
US07943622B2

Reaction notes

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