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Potassium Hydroxide → 5-Methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine

HRID 557238
Notes
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Reaction equation

HRID 557238 reaction equation
N[C:2]1[S:3][C:4]2[CH2:5][N:6]([CH3:11])[CH2:7][CH2:8][C:9]=2[N:10]=1.N([O-])=O.[Na+].[OH-].[K+]>S(=O)(=O)(O)O.[PH2](O)=O.O>[CH3:11][N:6]1[CH2:7][CH2:8][C:9]2[N:10]=[CH:2][S:3][C:4]=2[CH2:5]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 14797Potassium HydroxideHCID 23979985-methyl-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridin-2-amineHCID 23668193Sodium Nitrite

Product 1

HCID 111864405-Methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridineYield 67.5%

Reagents, catalysts & solvents 3

HCID 962WaterSolvent2×
HCID 1118
Sulfuric Acid
Solvent
HCID 4124402Phosphinic AcidSolvent

Procedure

2-Amino-5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine (10.00 g) was dissolved in a mixture of sulfuric acid (25 mL), hypophosphorous acid (50%, 13 mL), and water (100 mL) at 15 to 18° C., to thereby give an orange solution. To the solution was added dropwise a solution of sodium nitrite (8.15 g) in water (30 mL) at −2 to 3° C. over 30 minutes. After the resultant mixture was stirred at 0 to 10° C. for 2.5 hours, 8N aqueous potassium hydroxide (130 mL) was added dropwise thereto, and the pH was found to be 12.6. The precipitated potassium sulfate was filtered off, and was washed with ethyl acetate (200 mL). The aqueous layer was separated from the filtrate, and was further extracted with ethyl acetate twice (200 mL×2). The organic layers were combined, and the combined organic layer was dried over sodium sulfate anhydrate (30.00 g). After any insoluble material was filtered off and washed with ethyl acetate (100 mL), the filtrate was concentrated under reduced pressure, to thereby give 6.15 g of the title compound.

Workup

  1. customto thereby give an orange solution
  2. filtrationThe precipitated potassium sulfate was filtered off
  3. washwas washed with ethyl acetate (200 mL)
  4. customThe aqueous layer was separated from the filtrate
  5. extractionwas further extracted with ethyl acetate twice (200 mL×2)
  6. dry with materialthe combined organic layer was dried over sodium sulfate anhydrate (30.00 g)
  7. filtrationAfter any insoluble material was filtered off
  8. washwashed with ethyl acetate (100 mL)
  9. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-8c6d3ed6f98b4c869753310db3e2863b
Source dataset
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08058440B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes