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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245557Generated: November 2, 2026

Sodium Chloride → HCID 135462020, compound

https://huagongshe.com/reaction/2245557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantPhosphorus trichlorideHCID 24387—
ReactantSodium hydrideHCID 24758—
Reactant2-Oxindole-6-carbonitrileHCID 2773348—
ReactantHCID 11334324HCID 11334324—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
SolventChloroform ethylacetateHCID 21584013—
ProductHCID 135462020HCID 13546202015%

Reaction Steps

To a suspension of sodium hydride (97%, 0.024 g, 1.0 mmol) in N,N-dimethylformamide (1.5 mL) was added 2-oxoindoline-6-carbonitrile (0.119 g, 0.75 mmol). The resulting mixture was stirred for 5 min at room temperature and 1-[(6-chloro-1-oxidopyridin-3-yl)carbonyl]-4-methylpiperazine (0.128 g, 0.5 mmol) was added. The resulting reaction mixture was set under an N2 atmosphere and stirred for 20 h at room temperature. The N,N-dimethylformamide reaction solution was diluted with saturated aqueous sodium hydrogen carbonate and sodium chloride (2.0 g) was added followed by extractions with chloroform, ethyl acetate, and tetrahydrofuran. The combined organic extracts were dried (Na2SO4) and concentrated in vacuo. The remaining N,N-dimethylformamide was removed by co-evaporation with toluene (1×). The residual oil was dissolved in a chloroform/ethyl acetate, (5:1, 6 mL), and phosphorus trichloride (0.275 g, 2.0 mmol) was added. The reaction mixture was stirred for 60 min at 60° C., and was then cooled to room temperature. The mixture was poured into a saturated aqueous sodium hydrogen carbonate solution and sodium chloride (2.0 g) was added followed by extractions with chloroform (4×) and ethyl acetate (2×). The combined organic extracts were dried (Na2SO4) and concentrated in vacuo. Purification using preparative HPLC (XTerra®PrepMS C8 column 10 μm, 30×150 mm; 0.1 M NH4OAc buffer/acetonitrile, (80:20-20:80), as the eluent) gave 0.028 g (15% yield) of the title compound as the base. The base (0.025 g, 0.069 mmol) was dissolved in chloroform/methanol, (1:1), and treated with HCl in diethyl ether (1 M) at 0° C. The resulting yellow crystals were collected by filtration and washed with diethyl ether to obtain 0.020 g (70% yield) of the title compound: 1H NMR (DMSO-d6, 400 MHz) δ 10.61 (br s, 1H), 8.41 (s, 1H), 7.93 (br s, 1H), 7.80 (br s, 2H), 7.30 (br s, 1H), 7.15 (br s, 1H), 3.58 (br s, 4H), 2.40 (br s, 4H), 2.25 (s, 3H); MS (EI) m/z 362 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683067B2
Source datasetuspto-grants-2010_03
ORD IDord-e68a6bb16073467f806832d0df8177e6
Source noteuspto-grants-2010_03