HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4-[5-Bromo-4-(2-phenylethyl)-1,3-thiazol-2-yl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-[4-(2-Phenylethyl)-1,3-thiazol-2-yl]piperidine hydrochloride | HCID 67156883 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-[5-Bromo-4-(2-phenylethyl)-1,3-thiazol-2-yl]piperidine | HCID 67156856 | — |
Reaction Steps
At 0° C., bromine (123 mg) is added dropwise to a solution of 4-[4-(2-phenylethyl)-1,3-thiazol-2-yl]piperidine hydrochloride (II-1, 200 mg) in acetic acid (2 ml). The mixture is stirred for 30 min, and saturated sodium bicarbonate solution is then added. The aqueous phase is separated off and extracted with ethyl acetate. The combined organic phases are dried over anhydrous sodium carbonate, concentrated under reduced pressure and purified chromatographically. This gives 4-[5-bromo-4-(2-phenylethyl)-1,3-thiazol-2-yl]piperidine (127 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943774B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-4d4c8d0847f74031b15aa5dc3076e71e |
| Source note | uspto-grants-2011_05 |