HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1-Pentanol → 6-chloro-2-[1-[(4-chlorophenyl)methyl]-4-piperidinyl]-2,3-dihydro-1,3-dioxo-1H-isoindole-5-sulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1-Pentanol | HCID 6276 | — |
| Edukt | Phthalimide | HCID 6809 | — |
| Edukt | 4-(Aminosulfonyl)-5-chlorophthalimide | HCID 19733 | — |
| Edukt | 1-((4-Chlorophenyl)methyl)piperidin-4-amine | HCID 7130833 | — |
| Produkt | 6-chloro-2-[1-[(4-chlorophenyl)methyl]-4-piperidinyl]-2,3-dihydro-1,3-dioxo-1H-isoindole-5-sulfonamide | HCID 13370602 | — |
Reaktionsschritte
Reaction of 4-chloro-5-sulfamoylphthalimide (5.57 g., 0.0214 mole) and 4-amino-1-(4-chlorobenzyl)piperidine (4.8 g., 0.0214 mole) in 85 ml. of n-pentanol according to the procedure of Example 1(a) with heating at 130°-138° for a 48 hr. period afforded 7.07 g. (71%) m.p. 248°-250° (dec.) of the 1,3-dioxoisoindole product. A sample crystallized from dimethylformamide-methanol provided analytically pure 6-chloro-2-[1-[(4-chlorophenyl)methyl]-4-piperidinyl]-2,3-dihydro-1,3-dioxo-1H-isoindole-5-sulfonamide, m.p. 250°-251° (dec.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04600758 |
| Quelldatensatz | uspto-grants-1986_07 |
| ORD ID | ord-691cd2b016f94d458983ed72bf182b8c |
| Quellennotiz | uspto-grants-1986_07 |