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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301622Generated: October 30, 2026

N-((2S)-Tetrahydrofurfuryl)-6-chloro-2-hydroxy-3-nitrobenzenesulfonamide → HCID 69824535, compound

https://huagongshe.com/reaction/2301622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-((2S)-Tetrahydrofurfuryl)-6-chloro-2-hydroxy-3-nitrobenzenesulfonamideHCID 69824924—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
ProductHCID 69824535HCID 6982453594%

Reaction Steps

Following the general hydrogenation procedure outlined in example 15, N-((2S)-tetrahydrofurfuryl)-6-chloro-2-hydroxy-3-nitrobenzenesulfonamide (270 mg, 0.80 mmol) was reduced with hydrogen and Pd/C (140 mg) to form the desired product (226 mg, 94%). EI-MS m/z 305(M-H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500863B1
Source datasetuspto-grants-2002_12
ORD IDord-95e27785b5284ec5b2f7d2413c12aa32
Source noteuspto-grants-2002_12