HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727932Generated: October 26, 2026
3,3-Diphenylpropylamine → 4-[4-(3,5-Dichlorophenyl)-2,6-dimethyl-5-(3,3-diphenylpropylcarbamoyl)pyridine-3-carbonyl]piperazine-1-carboxylic acid t-butyl ester
https://huagongshe.com/reaction/1727932
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,3-Diphenylpropylamine | HCID 79698 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Diammonium cerium nitrate | HCID 14029277 | — |
| Reactant | 4-[5-Carboxy-4-(3,5-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3-carbonyl]piperazine-1-carboxylic acid t-butyl ester | HCID 69069674 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[4-(3,5-Dichlorophenyl)-2,6-dimethyl-5-(3,3-diphenylpropylcarbamoyl)pyridine-3-carbonyl]piperazine-1-carboxylic acid t-butyl ester | HCID 69070738 | — |
Reaction Steps
300 mg (0.588 mmol) of 4-[5-carboxy-4-(3,5-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3-carbonyl] piperazine-1-carboxylic acid t-butyl ester, 0.12 ml (0.882 mmol) of 3,3-diphenylpropylamine and 248 mg (1.29 mmol) of WSC hydrochloride were stirred in 15 ml of dichloromethane and 1 ml of DMF at room temperature overnight. After dichloromethane was evaporated under reduced pressure, ethyl acetate was added. After being washed with saturated aqueous sodium hydrogencarbonate solution and 1 N hydrochloric acid, the organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was dissolved in 8 ml of acetone. 811 mg (1.48 mmol) of diammonium cerium nitrate (IV) suspended in 8 ml of water was dropped and stirred at room temperature for 1 hour. After acetone was evaporated under reduced pressure, ethyl acetate was added. After being washed with water, the organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by the silica gel chromatography (dichloromethane/methanol=100/1 to 80/1) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07494989B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-73f47c53d179419ab3ee47aefb82086d |
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| Source note | uspto-grants-2009_02 |
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