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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076359Generated: October 30, 2026

Acetic Acid → HCID 25023595, compound

https://huagongshe.com/reaction/2076359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyrrolidineHCID 31268—
ReactantHCID 59397215HCID 59397215—
SolventTolueneHCID 1140—
SolventDichloromethane heptaneHCID 21907733—
ProductHCID 25023595HCID 25023595—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 2-benzyl-7-(2-fluoroethyl)-7-(3-oxobutyl)-7,8-dihydrocyclopenta[e]indazol-6(2H)-one (10.8 g, 28.6 mmol) in 300 mL of toluene were added pyrrolidine (2.4 mL, 28.6 mmol) and acetic acid (1.64 mL, 28.6 mmol) and the solution was heated at 90° C. under nitrogen. After 15 hours, the solution was cooled to room temperature and partitioned between EtOAc and water. The organic phase was washed with 5% aqueous NaHCO3 and brine and dried over MgSO4. Evaporation of the solvent under vacuum gave a brown oil which was purified by chromatography on silica gel (1:2 to 1:1 EtOAc/hexanes) to give a sticky orange solid. The solid was dissolved in heptane-dichloromethane and then most of the dichloromethane was evaporated under reduced pressure. The resulting precipitated solid was isolated by filtration to give 2-benzyl-9a-(2-fluoroethyl)-8,9,9a,10-tetrahydroindeno[2,1-e]indazol-7(2H) -one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923568B2
Source datasetuspto-grants-2011_04
ORD IDord-a76086e7fe90420a856cff39c463235a
Source noteuspto-grants-2011_04