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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047571Generated: October 30, 2026

Sodium Bisulfite → HCID 178429876, compound

https://huagongshe.com/reaction/1047571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BisulfiteHCID 23665763—
Reactant4-(2-Methylmorpholino)benzene-1,2-diamineHCID 68385027—
Reactant5-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehydeHCID 86673211—
CatalystHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178429876HCID 17842987655.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

5-Nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde (150 mg, 0.545 mmol) and 4-(2-methylmorpholino)benzene-1,2-diamine (113 mg, 0.545 mmol) were dissolved in THF (10 mL) and 2N HCl (1 drop) was added. The solution was heated at a gentle reflux for 30 min. Then, 1N sodium bisulfite (104 mg, 1 mmol; 2 mL of a 1N solution) was added and heated at reflux (70° C.) overnight. The solution was cooled to room temperature, and diluted with ethyl acetate (40 mL). The mixture was washed with water and brine, dried over Na2SO4, and concentrated. Purification by flash chromatography (5% CH3OH/CH2Cl2) afforded the title compound (140 mg). 1H NMR: (400 MHz, CDCl3): δ 9.56 (d, 1H, J=1.6 Hz), 8.28 (m, 1H), 7.74 (d, 1H, J=8.8 Hz), 7.64 (m, 1H), 7.36 (m, 1H), 7.03-6.96 (m, 1H), 5.75 (dd, 1H, J=2.8 and 6.4 Hz), 3.99 (m, 2H), 3.79 (m, 3H), 3.38 (m, 2H), 2.84 (m, 1H), 2.51 (m, 2H), 2.11 (m, 2H), 1.86 (m, 1H), 1.74 (m, 2H), 1.22 (d, 3H, J=6.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569511B2
Source datasetuspto-grants-2013_10
ORD IDord-328a7e4ea1074e7eb8da8750dcb862c4
Source noteuspto-grants-2013_10