참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-benzyl-N-methylpiperidin-4-amine | HCID 4136128 | — |
| 반응물 | 2-BROMO-3-ETHOXYPYRIDINE | HCID 10631926 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | U 99363 | HCID 133107 | — |
반응 단계
A mixture of N-(1-benzylpiperidin-4-yl)-N-methylamine (XXVII, 4.80 g) and 2-bromo-3-ethoxypyridine (XXVIIIa, 2.3805 g) is placed in a metal, screw cap reaction vessel using dichloromethane as the transfer solvent. Reduced pressure is applied to the vessel with heating at 50° to 60° for 45 min to remove dichloromethane. The vessel is then sealed and heated at 160 to 165° for 2 days. After cooling, the resulting solids are dissolved in dichloromethane and washed with water and saline. The organic phases are dried over magnesium sulfate and concentrated under reduced pressure to give the product, which is chromatographed (silica gel; eluting with ethyl acetate/hexane (30/70) followed by ethyl acetate/hexane (50/50)), to give N-(1-benzylpiperidin-4-yl)-N-(3-ethoxypyridin-2-yl)-methylamine (XXVIII, Chart G); MS (m/z) 325; IR (neat) 1462, 1211, 1481, 1589 and 1450 cm-1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06133446 |
|---|
| 출처 데이터셋 | uspto-grants-2000_10 |
|---|
| ORD ID | ord-b9ec82874c98434f919c817e0e47cfa8 |
|---|
| 출처 메모 | uspto-grants-2000_10 |
|---|