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4-Nitro-1H-indole → Methyl (4-nitro-1H-indol-3-yl)(oxo)acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Nitro-1H-indole | HCID 145766 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | Diphosphoryl tetrachloride | HCID 4432411 | — |
| 反応物 | HCID 86629729 | HCID 86629729 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Methyl (4-nitro-1H-indol-3-yl)(oxo)acetate | HCID 10243717 | — |
反応手順
Diphosphoryl chloride (0.938 mL, 6.80 mmol) was added dropwise to a solution of 4-nitroindole (1.00 g, 6.17 mmol) and methylpyrrolidinyl glyoxylate (Downie et al., Tetrahedron, 1993, 49, 4015-4034) (1.10 g, 6.80 mmol) at 0° C. and the mixture was allowed to warm to ambient temperature over 3 h. MeOH, then saturated aqueous NaHCO3 were added to the reaction at 0° C. and the solution was extracted with CH2Cl2 (3×50 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo until crystals formed. The crystals were collected by vacuum filtration and two more crops were isolated from the filtrate to give the title compound. MS: m/z=249 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07947677B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-e7bdc9ce3d3f4d53b12434c9a30abf3e |
| 出典メモ | uspto-grants-2011_05 |