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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887798Generated: October 30, 2026

methyl 9-(2-aminoethyl)-2-phenyl-8,9-dihydro-7H-cyclopenta[c]pyrazolo[1,5-a]pyridine-1-carboxylate → 2-(2-phenyl-8,9-dihydro-7H-cyclopenta[c]pyrazolo[1,5-a]pyridin-9-yl)ethanamine

https://huagongshe.com/reaction/887798

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 9-(2-aminoethyl)-2-phenyl-8,9-dihydro-7H-cyclopenta[c]pyrazolo[1,5-a]pyridine-1-carboxylateHCID 59145919—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
SolventSodium BicarbonateHCID 516892—
Product2-(2-phenyl-8,9-dihydro-7H-cyclopenta[c]pyrazolo[1,5-a]pyridin-9-yl)ethanamineHCID 59145877—

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl 9-(2-aminoethyl)-2-phenyl-8,9-dihydro-7H-cyclopenta[c]pyrazolo[1,5-a]pyridine-1-carboxylate (295 mg, 0.881 mmol) was dissolved in 40% (v/v) sulfuric acid (6 mL), and the mixture was stirred at 100° C. for 3 days. The reaction solution was diluted with water and neutralized with sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound. The obtained title compound was used for the reaction of Example 34 without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247429B2
Source datasetuspto-grants-2012_08
ORD IDord-284fe1f9459b4f649da7ac3fddf3b845
Source noteuspto-grants-2012_08