HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13986697, compound → HCID 13986699, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13986697 | HCID 13986697 | — |
| Reactant | HCID 131715265 | HCID 131715265 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 13986699 | HCID 13986699 | 67.2% |
Reaction Steps
A solution of 1.7 g of 2,3-dihydro-1,3-dioxo-1H -isoindole-alpha-methyl-acetyl chloride in 20 ml of dry dichloromethane was added dropwise to a solution of 2.0 g N-(2,6-dimethylphenyl)-3-pyridinehexanamine in 20 ml of dichloromethane. The reaction mixture was stirred overnight at room temperature, diluted with water and aqueous sodium hydroxide and the layers were separated. The aqueous layer was extracted with dichloromethane and the combined organic layers were washed with water, dried with potassium carbonate and concentrated. The residue was crystallized from ethyl acetate-hexane to give 2.3 g of rac.-2,3-dihydro-N-(2,6-dimethylphenyl)-alpha-methyl-1,3-dioxo-N-[6-(3-pyridinyl)hexyl]-1H-isoindole-2-acetamide, mp 113°-115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04891429 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-8396f7a0c77942648058a2c5b4d2fe2c |
| Source note | uspto-grants-1990_01 |