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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496153Generated: October 30, 2026

Ethylenediaminetetraacetic Acid → HCID 22324074, compound

https://huagongshe.com/reaction/496153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediaminetetraacetic AcidHCID 6049—
Reactant2-BromopyridineHCID 7973—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-5-iodobenzenesulfonamideHCID 22324088—
ReactantHCID 178418306HCID 178418306—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22324074HCID 2232407487%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of t-BuLi (1.7 M in pentane, 25 ml, 42 mmol) in dry THF at −78° C. was added 2-bromopyridine (1.9 ml, 20 mmol) in such a rate that the temperature did not exceed −70° C. The mixture was stirred for another 30 min at −78° C. A solution of ZnCl2 (2M in THF, 30 ml, 60 mmol) was added slowly and the cooling bath was removed and warmed to 20° C. 5-Iodo-2-aminobenzenesulfonamide (see compound 37) (1.0 g, 3.2 mmol) and Pd(PPh3)4 (0.3 g, 8 mol %) was added and the mixture was refluxed for 6 h. The THF was evaporated and the residue was treated with EDTA (53 g, 0.18 mol) and made slightly basic (pH=8-9) with 1 M NaOH followed by extraction with EtOAc (3×100 ml), drying (Na2SO4). The organic layer was concentrated to ca. 40 ml and n-hexane was added slowly. The product was filtered off, yielding 0.72 g (87%) of 2-amino-4-methyl-5-(2-pyridyl)-1-benzenesulfonamide as light-yellow crystals. The product was further transformed by Method G (using cyclohexanecarboxaldehyde). M.p. 229-231° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943159B1
Source datasetuspto-grants-2005_09
ORD IDord-32a8e5683b83495b92c26d5862630506
Source noteuspto-grants-2005_09