Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1H-Pyrazol-3-amine, 5-methyl- | HCID 93146 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178509299 | HCID 178509299 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178434099 | HCID 178434099 | 3.3% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875728B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-857e3f6c891140668e9cf7dc3ab33bc6 |
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| Source note | uspto-grants-2011_01 |
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