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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1932349Generated: October 26, 2026

3-Fluorobenzyl chloride → 1-(3-fluorobenzyl)-2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine hydrochloride

https://huagongshe.com/reaction/1932349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorobenzyl chlorideHCID 9974—
Reactant18-Crown-6HCID 28557—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridineHCID 67141589—
SolventTetrahydrofuranHCID 8028—
Product1-(3-fluorobenzyl)-2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine hydrochlorideHCID 6714286010%

Reaction Steps

18-Crown-6 (2.5 mg, 0.0097 mmol) and potassium tert-butoxide (33 mg, 0.291 mmol) were added to a solution of 2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine (24 mg, 0.097 mmol) prepared in Example 242 in anhydrous tetrahydrofuran (0.5 ml). The reaction mixture was stirred for 30 minutes at room temperature and 3-fluorobenzyl chloride (20 μl, 0.16 mmol) was added thereto. The reaction mixture was stirred overnight and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography. The resulting product was dissolved in ethyl acetate, saturated with hydrochloric acid gas, and then filtered to give 3.8 mg of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188114B2
Source datasetuspto-grants-2012_05
ORD IDord-01e2402302b5469084bfb478fc740561
Source noteuspto-grants-2012_05