참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | 1-(1-Naphthyl)ethanol | HCID 98030 | — |
| 반응물 | 4-(2-Bromo-5-methoxybenzyl)piperidine hydrochloride | HCID 22675334 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(2-(1-naphthyl)ethyl)-4-(2-bromo-5-methoxybenzyl)piperidine | HCID 12968873 | 81% |
반응 단계
Methanesulfonyl chloride (100 μl, 1.26 mmol) was added dropwise to a solution of 1-naphthylethanol (206 mg, 1.20 mmol) and triethylamine (350 μl, 2.40 mmol) in dichloromethane (2 ml) under ice-cooling and stirred for 3 hours. The solvent was distilled off and the resulting residue was dissolved in acetonitrile (3 ml) together with a base converted from 4-(2-bromo-5-methoxybenzyl)piperidine hydrochloride (384 mg, 1.20 mmol) according to the method described in Example 11, potassium iodide (199 mg, 1.20 mmol) and potassium carbonate (332 mg, 2.40 mmol). The resulting solution was heated under reflux for 3.5 hours and then allowed to cool. The precipitate was filtered off and the filtrate was concentrated, and then the residue was purified by a silica gel column chromatography (chloroform:methanol=20:1) to obtain the title compound (425 mg, 81%) as a light-brown solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06787560B2 |
|---|
| 출처 데이터셋 | uspto-grants-2004_09 |
|---|
| ORD ID | ord-42d154bb417940aa99b4d83fad8fa025 |
|---|
| 출처 메모 | uspto-grants-2004_09 |
|---|