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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium diazene-1,2-dicarboxylateHCID 6096233—
Reactant7-(2,4-dichloro-phenyl)-2-methyl-3-vinyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridineHCID 59811520—
SolventMethanolHCID 887—
Product7-(2,4-Dichloro-phenyl)-3-ethyl-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432283B2
Source datasetuspto-grants-2008_10
ORD IDord-4d7424b7128e4dca895cce1735779b69
Source noteuspto-grants-2008_10