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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814274Generated: November 2, 2026

HCID 87954650, compound → HCID 86588196, compound

https://huagongshe.com/reaction/1814274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 87954650HCID 87954650—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86588196HCID 8658819691.2%

Reaction Steps

A solution of N-methoxy-N-methyl-3-[2-(2-naphthalen-1-yl-ethoxy)-4-nitro-benzenesulfonylamino]-succinamic acid tert-butyl ester (0.52 g) in tetrahydrofuran (35 mL) and ethanol (35 mL) was treated with RaNi (0.3 g) and hydrogenated at 50 psi. The solution was filtered through Celite and evaporated to give the desired aniline derivative 3-[4-amino-2-(2-naphthalen-1-yl-ethoxy)-benzenesulfonylamino]-N-methoxy-N-methyl-succinamic acid tert-butyl ester (0.45 g) as an amorphous foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875765B2
Source datasetuspto-grants-2005_04
ORD IDord-f9e3920b52c34716b1876c005cb00b38
Source noteuspto-grants-2005_04