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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174062Generated: October 30, 2026

Potassium Hydroxide → HCID 178437482, compound

https://huagongshe.com/reaction/2174062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178437481HCID 178437481—
SolventEthanolHCID 702—
SolventHCID 86701559HCID 86701559—
ProductHCID 178437482HCID 178437482—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-(1-(5-ethyl-7-methyl-1-tosyl-1H-indol-4-yl)vinyl)-1H-benzo[d]imidazole-5-carbonitrile (79 mg, 0.164 mmol) and KOH (46.1 mg, 0.822 mmol) in EtOH (3 mL) was stirred at 100° C. for 0.5 h under the microwave irradiation. The reaction mixture was diluted with CH2Cl2/2,2,2-trifluoroethanol (c.a. 9/1). The mixture was washed with H2O, dried over Na2SO4, and filtered and concentrated. The resulting residue was purified by RP-HPLC (HC-A), then (HC-B) to give the title compound. 1H NMR (400 MHz, DICHLOROMETHANE-d2 with about 5 μL TFA) δ ppm 8.46 (br. s., 1H), 8.04 (s, 1H), 7.86 (d, J=8.59 Hz, 1H), 7.73 (dd, J=1.14, 8.59 Hz, 1H), 7.37 (s, 1H), 7.27 (t, J=2.80 Hz, 1H), 7.07 (s, 1H), 6.25 (s, 2H), 2.47-2.65 (m, 5H), 1.14 (t, J=7.45 Hz, 3H). HRMS calcd. for C21H18N4 (M+H)+ 327.1610. found 327.1612.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056874B2
Source datasetuspto-grants-2015_06
ORD IDord-c2c8751876624f4b9f1ba5913b5e8e9a
Source noteuspto-grants-2015_06