関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N,N-Dimethylaniline | HCID 949 | — |
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | Triethylamine hydrochloride | HCID 11130 | — |
| 生成物 | Benzenamine, N,N-dimethyl-, hydrochloride (1:1) | HCID 79987 | — |
反応手順
The aminations of Equations 43a and 43e are most conveniently effected by adding the requisite sulfonyl chlorides to a solution of the aminopyrazoles LIIa and LIIa' in a suitable solvent such as diethyl ether, tetrahydrofuran, or methylene chloride containing at least two equivalents of an acid scavenger such as triethylamine or dimethylaniline at temperatures between 0° C. and 65° C. The desired sulfonamides of Formulas LIIb and LIIb' are isolated either by filtration, in which case the by-product triethylamine hydrochloride or dimethylaniline hydrochloride is removed by washing with water, or extraction into a suitable organic solvent such as methylene chloride or ethyl acetate. Drying and evaporation of the solvent then affords the products LIIb and LIIb', which are usually sufficiently pure to be carried directly onto the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04707178 |
|---|
| 出典データセット | uspto-grants-1987_11 |
|---|
| ORD ID | ord-e8e56736969d488e907e0347c78e394e |
|---|
| 出典メモ | uspto-grants-1987_11 |
|---|