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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922378Generated: October 31, 2026

Hydrochloric Acid → HCID 86719346, compound

https://huagongshe.com/reaction/922378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Methylsulfonyl)piperazineHCID 709161—
Reactant6-Bromopyridine-2-carbaldehydeHCID 2757009—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86719346HCID 8671934620.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

A suspension of 6-bromopicolinaldehyde (1.50 g, 8.10 mmol), 1-(methylsulfonyl)piperazine (9, 5.30 g, 32.2 mmol), potassium carbonate (4.45 g, 32.2 mmol) and anhydrous DMF (10 mL) was placed in a sealed vessel and the mixture was heated at 120° C. for 20 h. The mixture was diluted with water (50 mL) and brought to pH 7 using 2 N aq. HCl (15 mL). The resulting solution was extracted with CH2Cl2 (3×50 mL) and the combined extracts were washed with brine (200 mL). The solution was dried (MgSO4), filtered, concentrated, and purified by silica gel chromatography eluting with 0-3% CH3OH in CH2Cl2 to afford the title compound (0.441 g, 20%) as an orange oil: 1H NMR (500 MHz, CDCl3) δ 9.90 (s, 1H), 7.67 (t, J=8.0 Hz, 1H), 7.34 (d, J=7.0 Hz, 1H), 6.89 (d, J=8.5 Hz, 1H), 3.80-3.78 (m, 4H), 3.37-3.33 (m, 4H), 2.81 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278940B2
Source datasetuspto-grants-2016_03
ORD IDord-7254a98b09cf4ec09bbfb039e1d8b9e8
Source noteuspto-grants-2016_03