Sulfuric Acid → HCID 178434099, compound

HRID 255016Notes

Reaction equation

HRID 255016 reaction equation
[NH2:1][C:2]1[NH:6][N:5]=[N:4][N:3]=1.S(=O)(=O)(O)O.[N:12]([O-])=O.[Na+].[NH2:16][C:17]1[CH:21]=[C:20]([CH3:22])[NH:19][N:18]=1>O.CC(O)=O>[CH3:22][C:20]1[C:21](=[N:12][NH:1][C:2]2[N:3]=[N:4][NH:5][N:6]=2)[C:17]([NH2:16])=[N:18][N:19]=1

Participants

7

Procedure

A solution of aminotetrazole (0.1 g, 1.1 mmol) in 4 M sulfuric acid (3.0 mL, 12.0 mmol) was cooled to −5° C. To this mixture was then added a cooled solution of sodium nitrite (0.08 g, 1.1 mmol) in 0.5 mL of water. The solution was then added to a solution of 3-amino-5-methylpyrazole (0.2 g, 2.1 mmol) and NaOAc trihydrate (1.5 g, 11 mmol) dissolved in a mixture of water (1 mL) and HOAc (3 mL). After stirring for 2 hours, water (50 mL) was added and the crude material was extracted from the aqueous layer three times with ethyl acetate (150 mL). The combined ethyl acetate solutions were washed with brine, dried over anhydrous MgSO4, filtered and evaporated. The crude material was purified by column chromatography (CHCl3:MeOH:NH4OH=3:1:0.005). The isolated material was then further purified by preparative TLC (CHCl3:MeOH:NH4OH=3:1:0.005) to yield 7 mg (3%) of the title compound as a red solid.

Workup

  1. extractionthe crude material was extracted from the aqueous layer three times with ethyl acetate (150 mL)
  2. washThe combined ethyl acetate solutions were washed with brine
  3. dry with materialdried over anhydrous MgSO4
  4. filtrationfiltered
  5. customevaporated
  6. customThe crude material was purified by column chromatography (CHCl3:MeOH:NH4OH=3:1:0.005)
  7. customThe isolated material was then further purified by preparative TLC (CHCl3:MeOH:NH4OH=3:1:0.005)

Sources & evidence

ORD record
ord-857e3f6c891140668e9cf7dc3ab33bc6
Source dataset
uspto-grants-2011_01
Patent number
US07875728B2

Reaction notes

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