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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261338Generated: November 3, 2026

Phenylacetyl isothiocyanate → N-(4-(1H-Pyrrolo[3,2-b]pyridin-7-yloxy)-3-fluorophenylcarbamothioyl)-2-phenyl acetamide

https://huagongshe.com/reaction/1261338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl isothiocyanateHCID 12454157—
Reactant4-(1H-Pyrrolo[3,2-b]pyridin-7-yloxy)-3-fluorobenzenamineHCID 59424593—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-(1H-Pyrrolo[3,2-b]pyridin-7-yloxy)-3-fluorophenylcarbamothioyl)-2-phenyl acetamideHCID 5942459140%

Reaction Steps

A mixture of 268 (20 mg, 0.08 mmol) and 2-phenylacetyl isothiocyanate (16 □L, 0.08 mmol) in THF (1 mL) was stirred at room temperature for 2 hours and concentrated. The residue was purified by flash column chromatography (eluent EtOAc) followed by preparative HPLC (column Aqusil C18, gradient elution with 60-95% MeOH in water, 45 min) to afford the title compound 269a (13 mg, 40% yield) as an off-white solid. 1H NMR (CD3OD) δ (ppm): 8.41(s, 1H), 8.16(d. 1H, J=5.6 Hz), 8.02(dd, 1H, J1=2.3 Hz, J2=12.2 Hz), 7.62(d, 1H, J=3.3 Hz), 7.44(m, 1H), 7.37-7.33(m, 4H) 7.31-7.26(m, 1H), 6.65(d, 1H, J=3.1 Hz), 6.52(d, 1H, J=5.7 Hz), 3.76(s, 2H), MS (m/z): 421.1(M+H) (found).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470850B2
Source datasetuspto-grants-2013_06
ORD IDord-918a25a83eab4efba42706b03be6c999
Source noteuspto-grants-2013_06