HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Aminosulfonyl)-5-chlorophthalimide → 1-Pentanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Aminosulfonyl)-5-chlorophthalimide | HCID 19733 | — |
| Reactant | 1-{[3-(Trifluoromethyl)phenyl]methyl}piperidin-4-amine | HCID 12888929 | — |
| Product | 1-Pentanol | HCID 6276 | — |
| Product | Phthalimide | HCID 6809 | — |
Reaction Steps
Reaction of 4-chloro-5-sulfamoylphthalimide (10.1 g., 0.0386 mole) and 4-amino-1-(3-trifluoromethylbenzyl)piperidine (10.0 g., 0.0386 mole) in 200 ml. of n-pentanol according to the procedure of Example 1(a) afforded the crude 1,3-dioxoisoindole product purified by chromatography to yield 8.1 g. (42% yield) of 6-chloro-2,3-dihydro-1,3-dioxo-2-[1-[[3-(trifluoromethyl)phenyl]methyl]-4-piperidinyl]-1H-isoindole-5-sulfonamide. The NMR spectral data was consistent for the compound used without further purification below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04495194 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-89c50013a4d74408a6bae3ee3d6af5fe |
| Source note | uspto-grants-1985_01 |