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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720447Generated: October 28, 2026

Bromide ion → HCID 21891474, compound

https://huagongshe.com/reaction/720447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant2-PiperidoneHCID 12665—
ReactantSodium hydrideHCID 24758—
ReactantPotassium BromideHCID 253877—
ReactantHCID 21891477HCID 21891477—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
ProductHCID 21891474HCID 2189147442%

Reaction Conditions

Temperature0 °C

Reaction Steps

Part C: 6-(4-Chloro-butyl)-1-(4-methoxy-phenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carbonitrile (0.148 g, 0.412 mmol) and potassium bromide (0.982 g, 8.24 mmol) were dissolved in acetone (25 mL) and refluxed overnight. The reaction was concentrated, quenched with water (100 mL), extracted with ethyl acetate (3×100 mL), washed with brine (1×100 mL), dried over MgSO4, concentrated, and purified by flash chromatography using 0–100% ethyl acetate/hexanes gradient as eluent to afford 0.136 g (82%). 2-Piperidone (0.136 g, 0.340 mmol) was dissolved in N,N-dimethylformamide (7 mL) and the reaction was cooled to 0° C. Sodium hydride (60%, 0.040 g, 1.01 mmol) was added and the reaction was stirred at 0° C. for 30 min. The bromide intermediate (0.136 g, 0.34 mmol) dissolved in N,N-dimethylformamide (8 mL) was added, and the reaction was stirred at rt overnight. The reaction was quenched with 1N hydrochloric acid (100 mL), extracted with ethyl acetate (3×100 mL), washed with water (100 mL), washed with brine (1×100 mL), dried over MgSO4, concentrated, and purified by flash chromatography using 0–100% ethyl acetate/hexanes gradient as the eluent. Further purification by reverse-phase HPLC and freeze-drying afforded 1-(4-methoxy-phenyl)-7-oxo-6-[4-(2-oxo-piperidin-1-yl)-butyl]-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carbonitrile (0.060 g, 42%). The carbonitrile (0.060 g, 0.141 mmol), 1N sodium hydroxide (10 mL), hydrogen peroxide (30%, 10 mL), and catalytic tetrabutyl hydrogen sulfate were dissolved in methylene chloride (10 mL) and stirred overnight at rt. The reaction was quenched with 1N sodium hydroxide (20 mL), concentrated to about 10 mL of solution, water (100 mL) added, extracted with ethyl acetate (3×100 mL), washed with brine (1×100 mL), dried over MgSO4, concentrated, and purified by reverse phase HPLC and freeze-dried to afford the title compound (0.034 g, 54%): 1H NMR (CHCl3) δ 7.45 (d, j=8.8 Hz, 2H), 6.97 (d, j=8.8 Hz, 2H), 6.82 (s, 3H), 5.44 (s, 3H), 3.85 (s, 3H), 3.65 (t, j=7.0 Hz, 2H), 3.49 (t, j=7.0 Hz, 2H), 3.36 (t, j=6.8 Hz, 2H), 3.22 (t, j=7.0 Hz, 4H), 2.38–2.34 (m, 2H), 1.79–1.76 (m, 4H), 1.64–1.57 (m, 4H) ppm; Mass Spec 440.3(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135469B2
Source datasetuspto-grants-2006_11
ORD IDord-5be03f9879b046a29a116a9184e47bf5
Source noteuspto-grants-2006_11