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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323610Generated: October 30, 2026

Methanesulfonic Acid → HCID 178492080, compound

https://huagongshe.com/reaction/323610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant6-Chloro-2-(4-methoxyanilino)-2,3,4,9-tetrahydro-1H-pyrrolo[3,4-b]quinoline-1,3,9-trioneHCID 21997699—
SolventMethanolHCID 887—
ProductHCID 178492080HCID 17849208044%

Reaction Steps

6-Chloro-2-(4-methoxyanilino)-2,3,4,9-tetrahydro-1H-pyrrolo[3,4-b]quinoline-1,3,9-trione (2.72 g, 7.40 mM) was stirred in methanol (200 mL), and methanesulfonic acid (50 mL) was added. The tan suspension was heated to reflux for 16 hours during which it turned yellow. This yellow suspension was cooled to room temperature and filtered (the filtrate was saved for use in Example 8). The collected solids were washed with methanol to give the title compound as a yellow powder (1.19 g, 44%), mp 371-373° C.; MS(CI): 370 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214826B1
Source datasetuspto-grants-2001_04
ORD IDord-5cfd63be364440b2b7d966e895ccec9f
Source noteuspto-grants-2001_04