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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227505Generated: November 2, 2026

Phosphinic Acid → 6-Bromo-3-(morpholin-4-ylsulfonyl)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/227505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphinic AcidHCID 4124402—
ReactantHCID 10250559HCID 10250559—
ReactantSodium NitriteHCID 23668193—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-3-(morpholin-4-ylsulfonyl)-1H-indole-2-carboxamideHCID 57756144—

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Bromo-7-amino-3-(morpholin-4-ylsulfonyl)-1H-indole-2-carboxamide (25 mg, 0.062 mmol, 1.0 equiv) was dissolved in 5 ml of tetrahydrofuran and cooled to 0° C. 1.3 mL of hypophosphorous acid (50% weight in water) was added, immediately followed by Cu2O (0.9 mg, 0.01 mmol, 0.1 equiv) and NaNO2 (21.4 mg, 0.31 mmol), and the reaction was stirred for 90 minutes. The reaction mixture was partitioned between dichloromethane and water and extracted four times with dichloromethane. The combined organic layers were dried (Na2SO4), filtered, and concentrated in vacuo. Purification by preparative reversed phase HPLC provided the titled compound. Proton NMR for the product was consistent with the titled compound. ESI+MS: 388.1 M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560546B2
Source datasetuspto-grants-2009_07
ORD IDord-59bbda793d17455d87323b149a116d88
Source noteuspto-grants-2009_07