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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370624Generated: November 1, 2026

tert-Butyl (4-aminophenyl)carbamate → {4-[4-(2-Chloro-phenyl)-5-oxo-4,5-dihydro-3,4,7,9,9b-pentaaza-cyclopenta[a]naphthalen-8-ylamino]-phenyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2370624

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (4-aminophenyl)carbamateHCID 688611—
Reactant4-(2-Chloro-phenyl)-8-methanesulfinyl-4H-3,4,7,9,9b-pentaaza-cyclopenta[a]naphthalen-5-oneHCID 68194757—
SolventEthyl AcetateHCID 8857—
Product{4-[4-(2-Chloro-phenyl)-5-oxo-4,5-dihydro-3,4,7,9,9b-pentaaza-cyclopenta[a]naphthalen-8-ylamino]-phenyl}-carbamic acid tert-butyl esterHCID 68194660—

Reaction Steps

A mixture of Example 1E (330.0 mg, 0.917 mmol) and tert-butyl 4-aminophenylcarbamate (306 mg, 1.468 mmol) was heated in a capped vial at 100° C. for 1 hour. The residue was dissolved in ethyl acetate and washed with saturated aqueous NaHCO3. The organic layer was dried over MgSO4, filtered, concentrated, and purified on a 40 g column using the ISCO Companion flash system eluting with hexane/ethyl acetate (5:5 to 4:6) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710065B2
Source datasetuspto-grants-2014_04
ORD IDord-525c9851b57e483d834f5f41e4ad2f6b
Source noteuspto-grants-2014_04