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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323633Generated: October 30, 2026

Methanesulfonic Acid → HCID 178489575, compound

https://huagongshe.com/reaction/323633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 21997679HCID 21997679—
SolventMethanolHCID 887—
ProductHCID 178489575HCID 17848957550%

Reaction Steps

A stirred suspension of 6-chloro-2-(2-methoxyanilino)-2,3,4,9-tetrahydro-1H-pyrrolo[3,4-b]quinoline-1,3,9-trione (1.78 g, 4.81 mM) in a solution of methanol (285 mL) and methanesulfonic acid (89 mL) was refluxed for 8 hours during which time a tan precipitate formed. The resulting suspension was cooled to room temperature and stirred for 16 hours. The suspension was filtered (the filtrate was saved for use in Example 30) and the collected solids were washed with methanol and then ether to give the title compound (0.889 g, 50%) as a yellow powder, mp 356-359° C.; MS(CI): 370 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214826B1
Source datasetuspto-grants-2001_04
ORD IDord-63a5aa61b5054b67b1ddeb78314df089
Source noteuspto-grants-2001_04