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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621202Generated: October 30, 2026

Acetic Acid → HCID 14233887, compound

https://huagongshe.com/reaction/621202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 14233885HCID 14233885—
ProductHCID 14233887HCID 14233887—

Reaction Steps

A solution of 1,2,3,9-tetrahydro-3-[hydroxy[5-methyl-1-(triphenylmethyl)-1H-imidazol-4-yl]methyl]-9-methyl-4H-carbazol-4-one (2.7070 g) in glacial acetic acid (100 ml) was treated with p-toluenesulphonic acid monohydrate (10.80 g) and the stirred solution heated at reflux for 4 h. The cool, dark liquid was evaporated, treated with aqueous saturated sodium bicarbonate (250 ml) and extracted into ethyl acetate (4×250 ml). The combined, dried organic extracts were evaporated, and purified by SPCC. Elution with System A (978:20:2→945:50:5) afforded the free base of the title compound as a light yellow-brown solid (488 mg). A hot solution of the free base (87 mg) in ethanol (ca. 16 ml) was treated with a hot solution of maleic acid (38 ml) in ethanol (1 ml), and on cooling the precipitate was collected to give the title compound (81 mg), m.p. 205°-209° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04822881
Source datasetuspto-grants-1989_04
ORD IDord-86bbc252b6014286928270b2aef9e501
Source noteuspto-grants-1989_04