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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602539Generated: October 29, 2026

Iodoethane → HCID 67152582, compound

https://huagongshe.com/reaction/602539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 67152479HCID 67152479—
ReactantHCID 68569164HCID 68569164—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67152582HCID 67152582—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3-[5-(2,6-diethyl-phenyl)-1-(4-isopropyl-phenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-propionic acid ethyl ester (120 mg, 0.25 mmol) in THF (3 mL) at −78° C. is added LDA (1.8 M solution in heptate/THF/ethylbenzene, 0.341 mL, 0.61 mmol). The mixture is stirred at −78° C. for 25 minutes and iodoethane (0.20 mL, 2.5 mmol) is added. The mixture is allowed to warm up to room temperature and stirred for 18 hours. To the mixture, an aqueous saturated NH4Cl solution (5 mL) is added, and THF is removed under reduced pressure. The product is extracted with EtOAc. The combined organic extracts are washed with brine, dried (Na2SO4), and concentrated under educed pressure. Chromatography of the residue on silica gel (Hexane/EtOAc, 4:1) gives 2-[5-(2,6-diethyl-phenyl)-1-(4-isopropyl-phenyl)-1H-pyrrolo[2,3-c]pyridin-3-ylmethyl]-2-ethyl-butyric acid ethyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906528B2
Source datasetuspto-grants-2011_03
ORD IDord-134c37da13824bd7bd44c9571e9e66fb
Source noteuspto-grants-2011_03