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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889724Generated: November 2, 2026

3,5-Dichloro-2-hydroxybenzenesulphonyl chloride → Methyl 6-((3,5-dichloro-N-(4-fluorobenzyl)-2-hydroxyphenylsulfonamido)-methyl)picolinate

https://huagongshe.com/reaction/1889724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichloro-2-hydroxybenzenesulphonyl chlorideHCID 90078—
ReactantMethyl 6-(((4-fluorobenzyl)amino)methyl)picolinateHCID 58531465—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 6-((3,5-dichloro-N-(4-fluorobenzyl)-2-hydroxyphenylsulfonamido)-methyl)picolinateHCID 5853136274.6%

Reaction Steps

To a solution of methyl 6-((4-fluorobenzylamino)methyl)picolinate (140 mg, 0.51 mmol) in THF (3 mL) were added 3,5-dichloro-2-hydroxybenzene-1-sulfonyl chloride (147 mg, 0.56 mmol) and TEA (0.142 mL, 1.02 mmol). The reaction mixture was stirred at rt overnight and concentrated in vacuo. The residue was purified by preparative HPLC. Fractions containing the desired product were combined, concentrated and lyophilized to give the desired product (0.19 g, 74%) as a white solid. 1H NMR (CD3OD) δ 7.93-7.80 (m, 2H), 7.65-7.53 (m, 3H), 7.27-7.25 (m, 2H), 6.94-6.90 (m, 2H), 4.68 (s, 2H), 4.65 (s, 2H), 3.98 (s, 3H). MS (ESI): 499.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-ebd99435d65740d2be33ac0712be262a
Source noteuspto-grants-2013_08