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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029512Generated: November 1, 2026

5-methyl-4-(methylamino)methyl-1-triphenylmethyl-1H-imidazole → HCID 19900737, compound

https://huagongshe.com/reaction/1029512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-methyl-4-(methylamino)methyl-1-triphenylmethyl-1H-imidazoleHCID 15308305—
Reactant4-methyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acidHCID 19900732—
SolventAcetonitrileHCID 6342—
ProductHCID 19900737HCID 19900737—

Reaction Steps

A mixture of 3.4 g (9.3 mmol) of 5-methyl-4-(methylamino) methyl-1-triphenylmethyl-1H-imidazole, 2.0 g (9.3 mmol) of 4-methyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid, and 2.06 g (10 mmol) of N,N-dicyclohexylcarbodiimide in 100 ml of acetonitrile was stirred for 12 hours under nitrogen. The precipitate was sucked off and the filtrate was evaporated in vacuo. The residue was dissolved in ethylacetate and washed with 2 N sodium hydroxide and saturated saline respectively, and then evaporated in vacuo. The residue was chromatographed on silicagel using methylene chloride/methanol (95/5) as an eluent. After evaporating the desired fractions 3.6 g of N-methyl, N-[(5-methyl-1-triphenylmethyl-1H-imidazol-4-yl)methyl]-4-methyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxamide were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102901
Source datasetuspto-grants-1992_04
ORD IDord-7ee14212a126443185592b0c574f4810
Source noteuspto-grants-1992_04