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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164409Generated: October 30, 2026

Phenyl 4-(carbamoylamino)-3-nitrobenzene-1-sulfonate → 5-Phenoxysulfonyl-2-ureidoaniline

https://huagongshe.com/reaction/2164409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl 4-(carbamoylamino)-3-nitrobenzene-1-sulfonateHCID 15585382—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Solvent2-MethoxyethanolHCID 8019—
Product5-Phenoxysulfonyl-2-ureidoanilineHCID 15585526—

Reaction Steps

33.7 g of 5-phenoxysulfonyl-2-ureidonitrobenzene in 250 ml of methanol and 250 ml of 2-methoxyethanol are hydrogenated under normal pressure with a catalytic amount of Raney nickel. After uptake of hydrogen is complete, the catalyst is filtered off with suction, washed with dimethylformamide and the solution is evaporated under reduced pressure, induced to crystallize with methanol, and the crystals are filtered off with suction and washed with methanol, melting point 180° C., decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04504490
Source datasetuspto-grants-1985_03
ORD IDord-71d78577a479446cb5eeb5b16ab49657
Source noteuspto-grants-1985_03