HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 178479774, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amine | HCID 10220561 | — |
| Reactant | HCID 13390872 | HCID 13390872 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178479774 | HCID 178479774 | — |
Reaction Steps
To a refluxing solution of 3-[3-(1-piperidinylmethyl)phenoxy]propylamine (0.870 g, 3.503 mmoles) in dried chloroform (35 ml) under dry nitrogen is added over 45 minutes a solution of 3-chloro-5-fluoro-1,2-benzisothiazole 1,1-dioxide (0.808 g, 3.679 mmoles) in dried chloroform (20 ml) while maintaining reflux. After the addition is complete refluxing is continued for 15 minutes and the solution allowed to come to room temperature. Evaporation in vacuo gives an orange solid. Recrystallization from isopropanol gives a light tan solid. m.p. 224°-226° after softening from 200° C. IR (KBr) 2950, 1600, 1302, 1171 cm-1 ; NMR (in DMSO) 1.76 (6H,s), 2.2 (2H,t), 2.8 (2H,m), 3.3 (3H,m), 3.6 (2H,t), 4.2 (3Hm,), 7.0-8.5 (7H,m), 10.1 (1h,s), 10.6 (1H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04490527 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-0a52d6250ca14a208065097e44985a12 |
| Source note | uspto-grants-1984_12 |