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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425510Generated: October 31, 2026

Triethylamine → HCID 16036824, compound

https://huagongshe.com/reaction/2425510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 291267HCID 291267—
Reactant(1S)-1-phenylpropan-1-amineHCID 6993773—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 16036824HCID 1603682471.3%

Reaction Steps

To a solution of 3-(methylthio)-2-phenylquinoline-4-carboxylic acid (150 mg, 0.51 mmol) and triethylamine (0.17 mL, 1.22 mmol) in EtOAc (2.5 mL) at 5° C. was added thionyl chloride (0.043 mL, 0.61 mmol). The cooling bath was removed and the suspension allowed to stir for 0.5 h, then (S)-(−)-1-phenylpropylamine (76 mg, 0.56 mmol) was added and reaction allowed to stir for another 0.5 h. Water (2 mL) and EtOAc (2 mL) were then added, the layers shaken together, then separated, the organics dried over Na2SO4, filtered, and concentrated under reduced pressure. The resulting material was purified by silica gel chromatography (0-20% EtOAc/CH2Cl2) to give the desired product (150 mg, 70% yield) as a solid. 1H NMR (300 MHz, CDCl3) δ 8.11 (d, J=8.4 Hz, 1H), 7.78-7.67 (m, 4H), 7.55-7.27 (m, 9H), 6.12 (d, J=8.5 Hz, 1H), 5.30 (q, J=7.6 Hz, 1H), 2.16-1.91 (m, 5H), 1.06 (t, J=7.4 Hz, 3H); HRMS m/z 413.1669, calcd 413.1688.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964733B2
Source datasetuspto-grants-2011_06
ORD IDord-93ed41bef03d491084f0783ce34c2f63
Source noteuspto-grants-2011_06