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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803849Generated: October 29, 2026

Thionyl Chloride → HCID 46244493, compound

https://huagongshe.com/reaction/1803849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-[(3-Dimethylamino-propyl)-methyl-amino]-2-nitro-benzoic acid hydrochlorideHCID 66737014—
Reactant5-[(3,5-difluorobenzyl)oxy]-1H-indazol-3-amineHCID 66997048—
CatalystDimethylformamideHCID 6228—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 46244493HCID 4624449364%

Reaction Conditions

Temperature4 °C

Reaction Steps

4-[(3-Dimethylamino-propyl)-methyl-amino]-2-nitro-benzoic acid hydrochloride (500 mg, 1.57 mmol) in dry THF (15 mL) was treated with one drop of DMF and with neat SOCl2 (0.34 mL, 4.69 mmol). The reaction mixture was refluxed for 0.5 hours, evaporated. The residue was taken in toluene (10 mL) and evaporated to dryness to afford a yellow solid that was suspended in dry pyridine (15 mL), cooled to 4° C. and treated with 5-(3,5-difluoro-benzyloxy)-1H-indazol-3-ylamine (360 mg, 1.31 mmol) in pyridine (5 mL). The solution was left at 4° C. over night and evaporated. The residue was dissolved in DCM (250 mL), washed with saturated NaHCO3 solution, water and brine. After drying over sodium sulfate and removal of the solvent, the crude was purified over silica gel (DCM: NH3 7N in MeOH 93:7) to afford 45 mg of title compound as an amorphous yellow solid (yield: 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354399B2
Source datasetuspto-grants-2013_01
ORD IDord-3c5540498d094a5dbba431a1a1eeb14c
Source noteuspto-grants-2013_01