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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647433Generated: October 29, 2026

HCID 20484885, compound → ethyl 2-[4-[N-(7-fluoroisoquinolin-3-yl)-N-methylamino]phenoxy}propionate

https://huagongshe.com/reaction/647433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20484885HCID 20484885—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Productethyl 2-[4-[N-(7-fluoroisoquinolin-3-yl)-N-methylamino]phenoxy}propionateHCID 2048490460.1%

Reaction Steps

Zinc powder (4×1.63 g) was added portionwise over a 2 hr period to a stirred solution of ethyl 2-{4-[N-(1-chloro-7-fluoroisoquinolin-3-yl)-N-methylamino]phenoxy}propionate (1.00 g) in acetic acid (50 ml). The mixture was filtered and the filter cake was washed with acetic acid. After the filtrate was evaporated the residue was partitioned between methylene chloride and water. The organic extract was washed successively with, aqueous sodium bicarbonate solution, water, aqueous ethylenediaminetetraacetic acid solution (5%) and water, then dried (MgSO4) and evaporated to give a green oil. Purification by column chromatography over silica gel (eluant dichloromethane) gave ethyl 2-[4-[N-(7-fluoroisoquinolin-3-yl)-N-methylamino]phenoxy}propionate (0.55 g) as a greenish oil. The assigned structure was confirmed by proton magnetic spectroscopy and mass spectrometry. Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 1.28 (3H, t); 1.64 (3H, d); 3.48 (3H, s); 4.25 (2H, q); 4.74 (1H, q); 6.62 (1H; s); 6.87-7.37 (7H, m); 8.85 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04409017
Source datasetuspto-grants-1983_10
ORD IDord-3efbcf8ab70e4e279937e3c865d54ac1
Source noteuspto-grants-1983_10