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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360746Generated: November 1, 2026

Toluene → HCID 25235943, compound

https://huagongshe.com/reaction/1360746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosgeneHCID 6371—
ReactantPiperidineHCID 8082—
Reactant3'-O-ethyl-N,N-diisopropylphosphoramiditeHCID 195451—
Reactant2-(2,6-Dichloro-phenyl)-3H-benzoimidazole-5-carboxylic acid hydrazideHCID 57786585—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 25235943HCID 25235943—

Reaction Conditions

Temperature150 °C

Reaction Steps

A 20% solution of phosgene in toluene (163 uL, 0.310 mmol) was added dropwise to a solution of piperidine (31 uL, 0.310 mmol) in DCM (2 mL) and EDIPA (108 uL, 0.620 mmol) at 0° C. under N2. The reaction was stirred for 40 min before the addition of 2-(2,6-dichloro-phenyl)-3H-benzoimidazole-5-carboxylic acid hydrazide (50 mg, 0.155 mmol) and DMF (1 mL). The ice in the ice bath was allowed to melt, slowly warming the reaction to room temp. The reaction was stirred for 4 days. The reaction was diluted with EtOAc (60 mL) and extracted with water (10 mL). The organic phase was concentrated to a yellow oil. The yellow oil was added to a microwave vial charged with THF (1.5 mL) and Burgess reagent. The mixture was heated by microwave irradiation to 150° C. for 15 min. The reaction was concentrated, and the concentrate diluted with water. The resulting precipitate was collected by filtration and purified by reverse-phase HPLC (25-60% ACN/H2O+5 mM NH4OH) to afford the title compound: 1H NMR (400 MHz, MeOD) δ ppm 1.74 (br. s., 6H) 3.57-3.64 (m, 4H) 7.55-7.63 (m, 3H) 7.78 (d, J=8.59 Hz, 1H) 7.94 (dd, J=8.53, 1.33 Hz, 1H) 8.20 (br. s., 1H); MS (m/z) 414.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879850B2
Source datasetuspto-grants-2011_02
ORD IDord-71bb07a31af9444da6bbee3e483d36aa
Source noteuspto-grants-2011_02