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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977213Generated: October 27, 2026

Methanesulfonic Acid → HCID 178515071, compound

https://huagongshe.com/reaction/1977213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 15512861HCID 15512861—
SolventMethanolHCID 887—
ProductHCID 178515071HCID 17851507143.1%

Reaction Steps

6-Chloro-2-(1-naphthylamino)-2,3,4,9-tetrahydro-1H-pyrrolo[3,4-b]quinoline-1,3,9-trione (1.30 g, 3.34 mM) was stirred in methanol (0.65 L) and methanesulfonic acid (65 mL) was added. The brown suspension was heated to reflux for 16 hours during which the solids dissolved to give a brown solution. This solution was cooled to room temperature. Addition of ice (10 mL) gave a tan suspension which was stirred for 1.5 hours. The suspension was filtered (the filtrate was saved for use in Example 24) and the collected solids were washed with methanol and ether to give the title compound (0.560 g, 43%) as a dull yellow pow der, mp 374-376° C.; MS(CI): 390 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232313B1
Source datasetuspto-grants-2001_05
ORD IDord-6152cae274544e76b481071ccf91706f
Source noteuspto-grants-2001_05