Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977209Generated: November 1, 2026

Methanesulfonic Acid → HCID 178426277, compound

https://huagongshe.com/reaction/1977209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant6-chloro-2-(4-methylanilino)-2,3,4,9-tetrahydro-1H-pyrrolo[3,4-b]quinoline-1,3,9-trioneHCID 21997718—
SolventMethanolHCID 887—
ProductHCID 178426277HCID 17842627737.1%

Reaction Steps

A stirred suspension of 6-chloro-2-(4-methylanilino)-2,3,4,9-tetrahydro-1H-pyrrolo[3,4-b]quinoline-1,3,9-trione (1.60 g, 4.53 mM) in a solution of methanol (128 mL) and methanesulfonic acid (32 mL) was refluxed for 4 hours and cooled to room temperature. The resulting yellow suspension was stirred at room temperature for five days and then filtered (the filtrate was saved for use in Example 19). The collected solids were washed with methanol and then ether to give the title compound (0.594 g, 37%) as a yellow powder, mp >400° C.; MS(CI): 354 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232313B1
Source datasetuspto-grants-2001_05
ORD IDord-fdead704a1c1437bb4d1953a06c3acea
Source noteuspto-grants-2001_05