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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824355Generated: October 31, 2026

Hydrochloric Acid → 6-Chloro-pyridine-3-sulfonic Acid [3-Chloro-4-(naphthalen-2-ylsulfanyl)phenyl]-amide

https://huagongshe.com/reaction/1824355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—
Reactant3,5-Dichloro-4-(napthalen-2-ylsulfanyl)-phenylamineHCID 22148834—
SolventTetrahydrofuranHCID 8028—
Product6-Chloro-pyridine-3-sulfonic Acid [3-Chloro-4-(naphthalen-2-ylsulfanyl)phenyl]-amideHCID 2351522358%

Reaction Steps

To a 0.35M solution of 3-chloro-4-(naphthalen-2-ylsulfanyl)-phenylamine (90)(150 mg, 0.53 mmol) in THF was added pyridine (Aldrich, 0.21 mL, 2.63 mmol) followed by 6-chloro-pyridine-3-sulfonyl chloride (Qorpark, 122 mg, 0.58 mmol). The resulting mixture was stirred for 15 hours. A 1M aqueous solution of HCl (20 mL) was added and the crude reaction mixture was extracted 3× with EtOAc (50 mL). The organic layers were combined and washed twice with a brine solution (100 mL), dried over Na2SO4, and concentrated under vacuum. The crude solid was chromatographed (5–15% EtOAc in hexane) to yield 140 mg (58%) of 94 as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041691B1
Source datasetuspto-grants-2006_05
ORD IDord-640771b625e849318f587d51732b5a01
Source noteuspto-grants-2006_05