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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106442Generated: October 31, 2026

4-Chlorobenzoic Acid → 9-(4-Chlorobenzoyl)-1,4,7,8,9,10-hexahydro-6-nitropyrido[3,4-f]quinoxaline-2,3-dione

https://huagongshe.com/reaction/1106442

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoic AcidHCID 6318—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,4,7,8,9,10-Hexahydro-6-nitropyrido[3,4-f]quinoxaline-2,3-dioneHCID 15434708—
Product9-(4-Chlorobenzoyl)-1,4,7,8,9,10-hexahydro-6-nitropyrido[3,4-f]quinoxaline-2,3-dioneHCID 21253061104.4%

Reaction Steps

The 7-nitroquinoxalinedione from Example 31 (100 mg, 0.38 mmol) was treated with the CDI adduct of 4-chlorobenzoic acid (0.57 mmol) by a procedure similar to that in Example 32 to give a yellow solid (159 mg, 99% yield). mp=280-283° C. (dec.). MS(CI) M+1 401; CHN calc'd for C18H13ClN4O5 within ±0.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057313
Source datasetuspto-grants-2000_05
ORD IDord-f3d3ac005b644ad3bedfd92f69a12922
Source noteuspto-grants-2000_05