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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586598Generated: October 31, 2026

Ammonia → HCID 21216864, compound

https://huagongshe.com/reaction/1586598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 86753910HCID 86753910—
SolventEthanolHCID 702—
ProductHCID 21216864HCID 21216864—

Reaction Steps

510 mg (1.08 mmol) 12-(3-Dimethylaminopropyl)-6,7,12,13-tetrahydro-3,9-dimethoxy-5,7-dioxoindolo-[2,3-a]furano[3.4-c]carbazole are heated in an autoclave for 24 hours at 140° C. in 40 ml of a saturated solution of ammonia in ethanol. After cooling, the precipitate obtained is filtered off with suction, chromatographed on silica gel with toluene/ethanol (10:1 v/v) and the fraction with the Rf 0.25 in toluene/ethanol (5:1 v/v) is isolated. 12-(3-Dimethylaminopropyl)-6,7,12, 13-tetrahydro-3,9-dimethoxy-5,7-dioxo-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazole is obtained in the form of yellow crystals which decompose from about 230° C. This compound can also be prepared from the same starting material by reaction with hexamethyldisilazane and methanol in dimethylformamide analogously to the process described in the literature (Tetrahedron Lett., 1990, 31, 5201).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05945440
Source datasetuspto-grants-1999_08
ORD IDord-695829c7ba8b4ff4890b73d0efeebd3a
Source noteuspto-grants-1999_08