HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 3-{1-(Cyclopropylmethyl)-4-piperidinyl}-1,2-benzisothiazole hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (Chloromethyl)cyclopropane | HCID 80013 | — |
| Reactant | 4-(3-Benzisothiazolyl) piperidine | HCID 13324093 | — |
| Reactant | Ether hydrobromide | HCID 86739792 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-{1-(Cyclopropylmethyl)-4-piperidinyl}-1,2-benzisothiazole hydrobromide | HCID 20255754 | 25% |
Reaction Steps
A stirred mixture of 5.0 g of 3-(4-piperidinyl)-1,2-benzisothiazole, 2.30 g of cyclopropylmethyl chloride, 7.95 g of potassium carbonate, 0.25 g of potassium iodide and 90 ml of dimethylformamide was heated at 90° for 20 hrs. The reaction mixture was poured into water and extracted with ethyl acetate. The organic extract was dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The oil was dissolved in ether and saturated hydrogen bromide/ether solution was added dropwise to precipitate the salt. The salt was recrystallized two times from ethyl acetate/ethanol to yield 2.0 g (25%) of product, mp 214°-216°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04524074 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-0d7b6b4ab3ef469f896c583ccb057d7a |
| Source note | uspto-grants-1985_06 |