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1-(1H-indol-3-yl)-2-methylpropan-2-amine → (R)-alpha-[[(1,1-dimethyl-2-(1H-indol-3-yl)ethyl)amino]methyl]tetrazolo[1,5-a]pyridine-6-methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(1H-indol-3-yl)-2-methylpropan-2-amine | HCID 9353 | — |
| 反応物 | (R)-2-(tetrazolo[1,5-a]pyrid 6-yl)oxirane | HCID 13090314 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (R)-alpha-[[(1,1-dimethyl-2-(1H-indol-3-yl)ethyl)amino]methyl]tetrazolo[1,5-a]pyridine-6-methanol | HCID 15137724 | — |
反応手順
A solution of 670 mg (3.58 mmol) of (1,1-dimethyl-2-(1H-indol-3-yl)ethyl amine (B. Heath-Brown and P. G. Philpott, J. Chem. Soc., 7165 (1965)) and 598 mg (3.69 mmol) of (R)-2-(tetrazolo[1,5-a]pyrid-6-yl)oxirane in 12 ml of absolute ethanol was heated at reflux for 15 hours. The reaction mixture was concentrated and the residue (1.24 g) chromatographed on silica gel (95:5:1 CH2Cl2 :MeOH:conc. NH4OH) to give 808 mg of (R)-α-[[(1,1-dimethyl-2-(1H-indol-3-yl)ethyl)amino]methyl]tetrazolo[1,5-a]pyridine-6-methanol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05030640 |
| 出典データセット | uspto-grants-1991_07 |
| ORD ID | ord-a86120e485ee4d11829d0b863349b470 |
| 出典メモ | uspto-grants-1991_07 |