HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113788Generated: November 1, 2026
Acetic Acid → 7-(2,4-Dichloro-phenyl)-3-ethyl-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridine
https://huagongshe.com/reaction/2113788
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium diazene-1,2-dicarboxylate | HCID 6096233 | — |
| Reactant | 7-(2,4-dichloro-phenyl)-2-methyl-3-vinyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridine | HCID 59811520 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-(2,4-Dichloro-phenyl)-3-ethyl-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridine | HCID 59811523 | — |
Reaction Steps
To a solution of 7-(2,4-dichloro-phenyl)-2-methyl-3-vinyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridine (3-7; 0.046 g, 0.15 mmol) in 2 mL of methanol was added dipotassium azodicarboxylate (0.174 g, 0.90 mmol) [prepared according to D. J. Pasto and R. J. Taylor, Organic Reactions 1991 40:91]. To the yellow suspension was added acetic acid (0.102 mL, 1.80 mmol) in 2 mL of methanol over 40 minutes. The reaction mixture was again treated with dipotassium azodicarboxylate (0.087 g, 0.45 mmol) and then acetic acid (0.051 mL, 0.90 mmol) in 1 mL of methanol over 20 nm. After 3 h at room temperature, the solvent was evaporated, the residue was treated with 10 mL of saturated sodium bicarbonate solution, extracted three times with 25 mL portions of dichloromethane, dried over magnesium sulfate, and evaporated to afford 41 mg of crude product. The crude product was purified by silica gel column chromatography eluting with 0 to 15% ethyl acetate/hexane which afforded 30 mg (65% theory) of 4-6 as a colorless oil: ms (M+H)+=310.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432283B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-4d7424b7128e4dca895cce1735779b69 |
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| Source note | uspto-grants-2008_10 |
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