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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535873Generated: October 30, 2026

Potassium Hydroxide → 7-(2-(6-(trifluoromethyl)pyridin-3-yl)ethyl)-2,3,5,6,7,11c-hexahydro-1H-pyrido[3',2':4,5]pyrrolo[2,3-g]indolizine

https://huagongshe.com/reaction/535873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant5-Ethenyl-2-(trifluoromethyl)pyridineHCID 57416848—
Reactant2,3,4,5,6,10c-hexahydro-1H-3a,6,7-triaza-cyclopenta[c]fluoreneHCID 67036606—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product7-(2-(6-(trifluoromethyl)pyridin-3-yl)ethyl)-2,3,5,6,7,11c-hexahydro-1H-pyrido[3',2':4,5]pyrrolo[2,3-g]indolizineHCID 67434028—

Reaction Steps

A solution of 2,3,5,6,7,11c-hexahydro-1H-pyrido[3′,2′:4,5]pyrrolo[2,3-g]indolizine (120 mg, 0.565 mmol) and powdered KOH (221.5 mg, 3.955 mmol) in NMP (2 mL) was stirred at RT for 10 min. 2-(Trifluoromethyl)-5-vinylpyridine (195.5 mg, 1.13 mmol) was added into the reaction mixture and stiffing continued for 24 h at RT. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue obtained was purified by silica gel flash chromatography to yield 7-(2-(6-(trifluoromethyl)pyridin-3-yl)ethyl)-2,3,5,6,7,11c-hexahydro-1H-pyrido[3′,2′:4,5]pyrrolo[2,3-g]indolizine;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859561B2
Source datasetuspto-grants-2014_10
ORD IDord-64a6b2a8352742d39e6497b71ea9a3a6
Source noteuspto-grants-2014_10