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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113045Generated: October 29, 2026

1,2-Dichloroethane → HCID 178426727, compound

https://huagongshe.com/reaction/2113045

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Benzylsulfonylamino-6-methyl-1-carboxymethyl-2-pyridinoneHCID 15458221—
Reactant4,5,6,7-tetrahydro-1H-indazol-5-amine dihydrochlorideHCID 178478653—
SolventDimethylformamideHCID 6228—
ProductHCID 178426727HCID 17842672738%

Reaction Steps

To a solution of 2-[3-[(benzylsulfonyl)amino]-6-methyl-2-oxo-1(2H)-pyridinyl]acetic acid (94.1 mg, 0.28 mmol) and 4,5,6,7-tetrahydro-2H-indazol-5-ylamine dihydrochloride (58.8 mg, 0.28 mmol) in 1 mL of DMF was added HOBt (42.8 mg, 0.28 mmol). The pH of the solution was adjusted to 8 with N-methylmorpholine and EDC (53.7 mg, 0.28 mmol) was added. The reaction mixture was stirred at room temperature overnight. The solvent was evaporated, and ethylacetate and saturated NaHCO3 solution were added to the residue. The water phase was extracted with ethyl acetate three times, and the combined organic phases were washed with saturated NaCl solution, dried over MgSO4, filtered and the solvent evaporated under reduced pressure. The product was purified by column chromatography (silicagel, eluant CH2Cl2/MeOH=9/1) to give 48 mg (38%) of a white solid compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524871B2
Source datasetuspto-grants-2009_04
ORD IDord-2ff7ddbf66af49bb9fd0d3b939db60d1
Source noteuspto-grants-2009_04