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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-methyl-4-(methylamino)methyl-1-triphenylmethyl-1H-imidazole | HCID 15308305 | — |
| Reactant | 4-methyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid | HCID 19900732 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19900737 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102901 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-7ee14212a126443185592b0c574f4810 |
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| Source note | uspto-grants-1992_04 |
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