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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432909Generated: October 29, 2026

Hydrochloric Acid → N-Cyclopropyl-5-(2,6-dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfonamide

https://huagongshe.com/reaction/432909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantCyclopropylamineHCID 69828—
Reactant5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfonyl chlorideHCID 15541442—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-Cyclopropyl-5-(2,6-dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfonamideHCID 1211418168.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled solution of 5-(2,6-dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfonyl chloride (920 mg, 2.2 mmol) in CH2Cl2 (25 mL) at 0° C. was added triethylamine (470 μL, 3.4 mmol) and cyclopropylamine (170 μL, 2.5 mol). The resulting mixture was stirred at 0° C. for 5 min, then at RT for 6 h. Water (30 mL) and 1N HCl (1 mL) was added and the solution was extracted with EtOAc (3×50 mL). The combined EtOAc extracts were dried and concentrated. The product was purified by chromatography to give the title compound of Step B (652 mg). MS (APCl) Calc.: 432.0, Found: 430.9 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664291B2
Source datasetuspto-grants-2003_12
ORD IDord-743a1107364c418a9b315b69b54a9955
Source noteuspto-grants-2003_12