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-(4-Methoxybenzyl)piperidin-4-amine | HCID 12641841 | — |
| Product | 1-Pentanol | HCID 6276 | — |
| Product | 6-Chloro-2,3-dihydro-2-[1-[(4-methoxyphenyl)methyl]-4-piperidinyl]-1,3-dioxo-1H-isoindole-5-sulfonamide | HCID 23312449 | — |
Reaction Steps
Reaction of 4-chloro-5-sulfamoylphthalimide (5.21 g., 0.02 mole) and 4-amino-1-(4-methoxybenzyl)piperidine (4.5 g., 0.02 mole) in 80 ml. of n-pentanol according to the procedure of Example 1(a) afforded the crude 1,3-dioxoisoindole product purified by chromatography (silica gel, ethyl acetate-n-hexane) to yield 2.88 g. (31%) of 6-chloro-2,3-dihydro-2-[1-[(4-methoxyphenyl)methyl]-4-piperidinyl]-1,3-dioxo-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 | US04600758 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-811d287b556843758a248cc3e7519b32 |
| Source note | uspto-grants-1986_07 |