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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900826Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3-(4-methoxybenzyl)-1-[(15-methyl-8-nitrotetracyclo[6.6.2.02,7.09,14]hexadeca-2,4,6,9,11,13-hexaen-15-yl)carbonyl]-1H-1,2,4-triazol-5-amine

https://huagongshe.com/reaction/900826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-(4-methoxybenzyl)-1H-1,2,4-triazol-3-amineHCID 5199320—
Reactant9-Nitro-9,10-dihydro-11-methyl-9,10-ethanoanthracene-11-carboxylic acidHCID 59698574—
SolventAcetonitrileHCID 6342—
Product3-(4-methoxybenzyl)-1-[(15-methyl-8-nitrotetracyclo[6.6.2.02,7.09,14]hexadeca-2,4,6,9,11,13-hexaen-15-yl)carbonyl]-1H-1,2,4-triazol-5-amineHCID 5867032788.3%

Reaction Steps

To a stirred solution of 15-methyl-8-nitrotetracyclo[6.6.2.02,7.09,14]hexadeca-2,4,6,9,11,13-hexaene-15-carboxylic acid (25 mg, 0.08 mmol, prepared according to WO04009017), 1-hydroxybenzotriazole (16 mg, 0.12 mmol), and N-ethyl-N,N-diisopropylamine (0.1 mL) in anhydrous acetonitrile (1 mL) was added EDCI (38 mg, 0.2 mmol) at RT under argon. After the mixture was stirred at RT for 5 min, 5-(4-methoxybenzyl)-1H-1,2,4-triazol-3-amine (21 mg, 0.1 mmol) was added. The reaction mixture was stirred at RT overnight and at 80° C. for 1 h. After the solvents were removed, the residue was partitioned between methylene chloride and saturated aqueous sodium bicarbonate solution. The aqueous solution was extracted with methylene chloride. The combined organic solutions were dried (Na2SO4), concentrated and purified by silica gel chromatography to give 35 mg (87% yield) of the title compound as a white solid. (M+H)+=496.20

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361654B2
Source datasetuspto-grants-2008_04
ORD IDord-d7fbef7174d34eb8b9d940750a961972
Source noteuspto-grants-2008_04