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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968735Generated: October 27, 2026

Acetic Acid → (7-Chloro-2-dimethylaminomethyl-quinolin-8-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/1968735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylamineHCID 674—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(7-Chloro-2-formyl-quinolin-8-yl)-acetic acid ethyl esterHCID 86253926—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(7-Chloro-2-dimethylaminomethyl-quinolin-8-yl)-acetic acid ethyl esterHCID 6688245778%

Reaction Steps

Dimethylamine (5.6 M solution in EtOH, 0.27 ml, 1.54 mmol, 1.5 equiv) was added to a solution of (7-chloro-2-formyl-quinolin-8-yl)-acetic acid ethyl ester (285 mg, 1.03 mmol) in anhydrous THF (5 ml). The reaction mixture was stirred at room temperature for 18 hours. A solution of NaCNBH3 (77 mg, 1.23 mmol, 1.2 equiv) in methanol (2 ml) was added, immediately followed by the addition of acetic acid (308 mg, 5.13 mmol, 5.0 equiv). After 5 minutes at room temperature, TLC analysis indicated complete conversion. The reaction mixture was diluted with water, adjusted to pH=8 with concentrated aqueous NaHCO3 solution, and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified via flash chromatography (gradient of CH2Cl2/MeOH 99:1 to 90:10) to afford the title compound (245 mg, 78%) as a colorless solid. 1H NMR (400 MHz, d6-DMSO): δ=8.45 (d, J=8.1 Hz, 1H), 7.98 (d, J=8.4 Hz, 1H), 7.69 (d, J=8.4 Hz, 1H), 7.63 (d, J=8.1 Hz, 1H), 4.47 (s, 2H), 4.08 (q, J=7.3 Hz, 2H), 2.50 (s, 6H), 1.16 (t, J=7.3 Hz, 3H). MS (ES+): 307.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426440B2
Source datasetuspto-grants-2013_04
ORD IDord-68d2b3cf3d3a4480bebb700b05e1008b
Source noteuspto-grants-2013_04