HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanesulfonylchloride, 2-chloro- → (4aS,8aR)-4-(3,4-Dimethoxy-phenyl)-2-(1-ethenesulfonyl-piperidin-4-yl)-4a,5,8,8a-tetrahydro-2H-phthalazin-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (4aS,8aR)-4-(3,4-Dimethoxy-phenyl)-2-piperidin-4-yl-4a,5,8,8a-tetrahydro-2H-phthalazin-1-one | HCID 68878852 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4aS,8aR)-4-(3,4-Dimethoxy-phenyl)-2-(1-ethenesulfonyl-piperidin-4-yl)-4a,5,8,8a-tetrahydro-2H-phthalazin-1-one | HCID 69797859 | — |
Reaction Steps
A solution of 20 mmol of 2-chloroethylsulfonylchloride in 20 ml of dichloromethane is added to a solution of 15 mmol of compound 5c and 25 ml of diisopropylethylamine in 50 ml of dichloromethane. The resulting mixture is stirred at RT for 18 h, after which it is washed first with diluted hydrochloric acid and then with a saturated solution of sodium bicarbonate. After drying over magnesium sulfate and evaporating the solvent, the compound is crystallised from diethyl ether. M. p. 89-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06933296B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-799bc06de1904f08b86ceebb0e10b122 |
| Source note | uspto-grants-2005_08 |