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[2-(4-Benzyloxyphenyl)-ethyl]-carbamic acid 4-nitrophenyl ester → 1-[2-(4-benzyloxyphenyl)ethyl]-3-{2-[2-(3,5-dimethylphenyl)-1H-indol-3-yl]ethyl}urea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | [2-(4-Benzyloxyphenyl)-ethyl]-carbamic acid 4-nitrophenyl ester | HCID 11429281 | — |
| 反応物 | 2-[2-(3,5-dimethylphenyl)-1H-indol-3-yl]ethylamine | HCID 22100919 | — |
| 生成物 | 1-[2-(4-benzyloxyphenyl)ethyl]-3-{2-[2-(3,5-dimethylphenyl)-1H-indol-3-yl]ethyl}urea | HCID 18914277 | 95.6% |
反応手順
To a solution of 2-[2-(3,5-dimethylphenyl)-1H-indol-3-yl]ethylamine (EXAMPLE 2 Step D, 39 mg in 1 mL dry methanol) was added 64 mg [2-(4-benzyloxyphenyl)-ethyl]-carbamic acid 4-nitrophenyl ester and the mixture stirred at room temperature. After 24 hours, the mixture was concentrated in vacuo and the residue re-solvated in ethyl acetate. This was washed with saturated aqueous potassium carbonate (3×) and brine, dried over sodium sulfate and purified by flash chromatography on silica gel (hexane:ethyl acetate, 5:4; then 1:1) to give the title compound (73 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05756507 |
| 出典データセット | uspto-grants-1998_05 |
| ORD ID | ord-45c7845f7acc49a5a87deeca9bbb99aa |
| 出典メモ | uspto-grants-1998_05 |