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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551137Generated: November 1, 2026

Triethylamine → HCID 59829687, compound

https://huagongshe.com/reaction/551137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenoxyacetyl chlorideHCID 69703—
ReactantHCID 59829670HCID 59829670—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59829687HCID 5982968726.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of 2-[8-(benzyloxy)-5-chloroquinolin-7-yl]-1-{5-[(dimethylamino)methyl]-2-furyl}ethanamine (0.431 mmol) and triethylamine (0.474 mmol, 1.1 eq.) in tetrahydrofuran (4 mL) at 0° C. was added phenoxyacetyl chloride (0.474 mmol, 1.1 eq.) and the resulting solution was stirred 5 min at 0° C. then warmed to room temperature and stirred 15 min. The reaction was quenched with saturated aqueous sodium bicarbonate solution (15 mL) and the resulting aqueous solution was extracted with ethyl acetate (3×10 mL). The combined organic layers were dried (MgSO4), filtered and concentrated to a white foam that was purified by column chromatography using 10% methanol/dichloromethane to give the final product as a clear oil (0.113 mmol, 26%). MS (ESI) m/z 570.3; HRMS: calcd for C33H32ClN3O4+H+, 570.21541; found (ESI, [M+H]+ Obs'd), 570.2155.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947712B2
Source datasetuspto-grants-2011_05
ORD IDord-aa297bed209a48ccb5e9bb645d2890ad
Source noteuspto-grants-2011_05