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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922465Generated: October 30, 2026

phenyl 2-(6-amino-8-fluoro-3,4-dihydroquinolin-1(2H)-yl)ethyl(methyl)carbamate → HCID 178484205, compound

https://huagongshe.com/reaction/1922465

Reaction equation

Participants

RoleNameHCIDCharge
Reactantphenyl 2-(6-amino-8-fluoro-3,4-dihydroquinolin-1(2H)-yl)ethyl(methyl)carbamateHCID 59807114—
ReactantMethyl thiophene-2-carbimidothioate hydroiodideHCID 66704664—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventSodium CarbonateHCID 10340—
ProductHCID 178484205HCID 17848420575.2%

Reaction Steps

To a stirred solution of phenyl 2-(6-amino-8-fluoro-3,4-dihydroquinolin-1(2H)-yl)ethyl(methyl)carbamate (426 mg, 1.241 mmol) in ethanol (12 ml) was added methyl thiophene-2-carbimidothioate hydroiodide (708 mg, 2.481 mmol). The reaction mixture was stirred at room temperature overnight under argon. The reaction mixture was then diluted with water and sodium carbonate, then extracted with dichloromethane (3×). The combined organics were dried, filtered and concentrated, then chromatographed in 40-100% ethyl acetate in hexanes, giving the desired phenyl 2-(8-fluoro-6-(thiophene-2-carboximidamido)-3,4-dihydroquinolin-1(2H)-yl)ethyl(methyl)carbamate 52 (422 mg, 0.933 mmol, 75% yield). 1H NMR (DMSO-d6) δ 7.74-7.71 (m, 1H); 7.59-7.57 (m, 1H); 7.41-7.36 (m, 2H); 7.23-7.18 (m, 1H); 7.14-7.07 (m, 3H); 6.50-6.42 (m, 3H); 6.37 (s, 1H); 3.62 (t, J=6 Hz, 1H); 3.51 (t, J=6 Hz, 1H); 3.30 (t, J=6 Hz, 1H); 3.23 (t, J=6 Hz, 1H); 3.15-3.09 (m, 2H); 3.09, 2.97 (2s, 3H); 2.69 (t, J=6 Hz, 2H); 1.83-1.75 (m, 2H). EI-MS (m/z, %): 452 (M+, 8); 288 (60); 179 (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173813B2
Source datasetuspto-grants-2012_05
ORD IDord-ee26eabd62b346d1950eb8946daf81a5
Source noteuspto-grants-2012_05