HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → 5,5-Dimethyl-8-(1,2-dimethylheptyl)-10-(4-piperidinobutyrylamino)-5H-[1]benzopyrano [4,3-c]pyridine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-(Piperidin-1-yl)butanoic acid hydrochloride | HCID 13172081 | — |
| Reactant | 10-Amino-5,5-dimethyl-8-(1,2-dimethylheptyl)-5H-[1]benzopyrano[4,3-c]pyridine | HCID 20309734 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5,5-Dimethyl-8-(1,2-dimethylheptyl)-10-(4-piperidinobutyrylamino)-5H-[1]benzopyrano [4,3-c]pyridine hydrochloride | HCID 131711222 | — |
Reaction Steps
A mixture of 0.87 g. (2.47 mmole) of 10-amino-5,5-dimethyl-8-(1,2-dimethylheptyl)-5H-[1]benzopyrano[4,3-c]-pyridine, 0.51 g. (2.47 mmole) of 4-piperidinobutyric acid hydrochloride, 0.56 g. (2.72 mmole) of dicyclohexylcarbodiimide, and 50 ml. of dry methylene chloride was stirred at room temperature for 72 hours. The mixture was cooled and filtered and the filtrate concentrated to a residue which was recrystallized from methylene chloride-ether, m.p. 185-186°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04111942 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-115b97623b824b87960db21a7c5ed223 |
| Source note | uspto-grants-1978_09 |