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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475552Generated: October 30, 2026

2-(4-Fluorophenyl)acetyl isothiocyanate → HCID 57967274, compound

https://huagongshe.com/reaction/1475552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Fluorophenyl)acetyl isothiocyanateHCID 23153248—
Reactant4-(2-(5-(1,3-Dioxan-2-yl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluoroanilineHCID 57967258—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 57967274HCID 5796727474.6%

Reaction Steps

To a solution of 2 (2.69 g, 13.80 mmol) in toluene (16.5 mL) and ethanol (16.5 mL) was added a suspension of 31 (4.87 g, 11.50 mmol) in toluene (41 mL) and ethanol (41 mL). The mixture was stirred for 1 h at room temperature and concentrated under reduced pressure. The residue was purified by flash column chromatography (eluent EtOAc/MeOH, 98/2) to afford intermediate 32 (5.31 g, 8.58 mmol, 74% yield) as a beige solid. MS (m/z): 619.2 (M+H). 1H NMR (400 MHz, DMSO-d6) δ (ppm): 12.47 (s, 1H), 11.83 (s, 1H), 8.63 (d, J=2.0 Hz, 1H), 8.54 (d, J=5.2 Hz, 1H), 8.38 (s, 1H), 8.28 (d, J=8.0 Hz, 1H), 8.02 (dd, J=12.4, 1.6 Hz, 1H), 7.92 (dd, J=8.2, 1.8 Hz, 1H), 7.54-7.52 (m, 2H), 7.37 (dd, J=8.6, 5.8 Hz, 2H), 7.17 (t, J=9.0 Hz, 2H), 6.68 (d, J=5.2 Hz, 1H), 5.66 (s, 1H), 4.18 (dd, J=10.6, 5.0 Hz, 2H), 3.97-3.94 (m, 2H), 3.82 (s, 2H), 2.10-1.98 (m, 1H), 1.47 (dd, J=14.0, 1.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018378B2
Source datasetuspto-grants-2015_04
ORD IDord-daf115957d2c49359e05e83d16d1bb6b
Source noteuspto-grants-2015_04