化工社化工社 化学情報印刷レポート · 研究参考用
HRID 236530作成日:2026年10月26日
2-Amino-4-methoxy-6-methyl-1,3,5-triazine → 4-Bromo-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-aminocarbonyl]-3-thiophenesulfonamide
https://huagongshe.com/reaction/236530
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine | HCID 15466 | — |
| 反応物 | 4-Bromothiophene-3-sulfonyl isocyanate | HCID 20215704 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-Bromo-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-aminocarbonyl]-3-thiophenesulfonamide | HCID 13203334 | — |
反応手順
To 1.1 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine in 20 ml of tetrahydrofuran was added 2 g of 4-bromo-3-thiophenesulfonyl isocyanate in 5 ml of tetrahydrofuran. The mixture was then stirred and warmed on a steam bath for 15 minutes and allowed to stir at ambient temperature for 70 hours. It was then heated to reflux for 2 hours, cooled to 10° C., filtered and the filtrate evaporated. The residual oil was triturated to yield the desired product as a solid which after recrystallization from acetonitrile melted at 180°-183°, yield 1.5 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04645529 |
|---|
| 出典データセット | uspto-grants-1987_02 |
|---|
| ORD ID | ord-7827bacfa57d43fd80f1ddda899307f7 |
|---|
| 出典メモ | uspto-grants-1987_02 |
|---|