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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534582Generated: October 30, 2026

Triethylamine → HCID 22914784, compound

https://huagongshe.com/reaction/1534582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
ReactantCarbonochloridateHCID 21226386—
Reactant8-Chloro-11-(1-methylpiperidin-4-ylidene)-11H-benzo[5,6]cyclohepta[1,2-b]pyridineHCID 22914786—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 22914784HCID 2291478456.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 755 mg (2.34 mmole) of 8-chloro-11-(1-methyl-4-piperidylidene)-11H-benzo[5,6]cyclohepta[1,2-b]pyridine and 1.5 mL of triethylamine in 25 mL of dry toluene at room temperature and under a nitrogen atmosphere was added 650 μL (4.72 mmole) of 2,2,2-trichloroethyl chloroformate. The mixture was then heated to 90° C. Additional amounts of the chloroformate (500 μL and 300 μL) and triethylamine (1.0 mL each time) were added to the mixture after 2 hr. and 3 hr. 40 min., respectively. After a total reaction time of 5 hr. the mixture was poured into water and extracted three times with CH2Cl2. The combined organic portions were dried over MgSO4, filtered and concentrated in vacuo. The residue was purified via flash chromatography [11/2% MeOH in CH2Cl2 ] to afford 639 mg (56%) of the title compound as a glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089496
Source datasetuspto-grants-1992_02
ORD IDord-b4c1e48b16954883bc8f6116d956a546
Source noteuspto-grants-1992_02