HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355933Generated: October 30, 2026
Triethylamine → N-[4-[(4,5-Dihydro-2-methylpyrazolo[4,3-d] [1]benzazepin-6(2H)-yl)carbonyl]phenyl]-2-methylbenzamide
https://huagongshe.com/reaction/355933
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methylbenzoyl chloride | HCID 70276 | — |
| Reactant | 2,4,5,6-Tetrahydro-2-methyl-6-(4-aminobenzoyl)-pyrazolo[4,3-d][1]benzazepine | HCID 53890129 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[4-[(4,5-Dihydro-2-methylpyrazolo[4,3-d] [1]benzazepin-6(2H)-yl)carbonyl]phenyl]-2-methylbenzamide | HCID 9932748 | — |
Reaction Steps
To a mixture of 0.420 g of 2,4,5,6-tetrahydro-2-methyl-6-(4-aminobenzoyl)pyrazolo[4,3-d][1]-benzazepine and 275 μl of triethylamine in 6 ml of methylene chloride and 2 ml of dioxane is added a solution of 215 μl of 2-methylbenzoyl chloride in 1.5 ml of dioxane. The reactants are stirred under argon for 4.5 hours. The volatiles are evaporated in vacuo to a residue which is dissolved in methylene chloride and washed with 10% NaHCO3 and brine. The organic layer is treated with activated carbon, dried with MgSO4 and evaporated an vacuo to give 660 mg of a tan foam residue. The residue is purified by column chromatography on silica gel by elution with 30% ethyl acetate-methylene chloride to give 590 mg of the desired product as white crystalline solid, m.p. 246°-248° C.; HR FABMS: (M+H)=437.1972.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834461 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-c9869784abb84e1ea4426766fbc6634b |
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| Source note | uspto-grants-1998_11 |
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