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1-(Bromomethyl)-2-phenylbenzene → 2-[1,1'Biphenyl]-2-yl-1-[4-(phenylmethyl)morpholin-2-yl]-1-tetrahydro-2H-pyran-4-ylethanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(Bromomethyl)-2-phenylbenzene | HCID 263365 | — |
| 反応物 | (4-benzylmorpholin-2-yl)(tetrahydro-2H-pyran-4-yl)methanone | HCID 59789303 | — |
| 反応物 | HCID 178419666 | HCID 178419666 | — |
| 生成物 | 2-[1,1'Biphenyl]-2-yl-1-[4-(phenylmethyl)morpholin-2-yl]-1-tetrahydro-2H-pyran-4-ylethanol | HCID 58854907 | — |
| 生成物 | HCID 178419666 | HCID 178419666 | — |
反応手順
Compound 55 is prepared from 8 (0.56 g, 1.94 mmol) and 2-phenyl benzyl magnesium bromide solution (0.25 M solution in diethyl ether, 9.31 mL, 2,33 mmol, 1.2 eq) following General Procedure 2. 2-Phenylbenzyl magnesium bromide is prepared from commercially available (Aldrich) 2-phenylbenzyl bromide following General Procedure 5. Further 2-phenyl benzyl magnesium bromide solution (1 mL) is added and the reaction left under stirring overnight. Purification by ion exchange chromatography gives 55 as an off-white foam-like solid (0.37 g, 68%). MW 457.62; C30H35NO3; LCMS. (6 minute method): m/z 458 [M+H]+, RT 3.58 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07423037B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-ca69a0b3786d4eeab4cf3763ad020698 |
| 出典メモ | uspto-grants-2008_09 |