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Methyl iodide → HCID 19805516、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | Allylamine | HCID 7853 | — |
| 反応物 | HCID 19805425 | HCID 19805425 | — |
| 反応物 | 4-Hydroxy-2-nitrobenzoic acid | HCID 21753345 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | HCID 19805516 | HCID 19805516 | 33% |
反応手順
Using a similar procedure to that described in Examples 2-16, but starting from N-allyl-4-methoxy-2-nitrobenzamide (itself prepared from 4-hydroxy-2-nitrobenzoic acid using the procedure described in the portion of Example 82 which is concerned with the preparation of starting material except that methyl iodide was used in place of butyl iodide and allylamine was used in place of benzylamine), using a mixture of ethanol and water (4/1 v/v) in place of aqueous methanol as the reaction solvent and having a reaction duration of 3 hours, there was obtained 1,2-dihydro-2-allyl-6-methoxy-3H-indazol-3-one (Ex. 178) as a solid, m.p. 126° C. in 33% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05173496 |
| 出典データセット | uspto-grants-1992_12 |
| ORD ID | ord-bb3eb66274b8410bbaca17da251f005a |
| 出典メモ | uspto-grants-1992_12 |