化工社化工社 化学情報印刷レポート · 研究参考用
HRID 326327作成日:2026年10月25日
Triethylamine → Isopropyl 2-chloro-4-fluoro-5-[(6-methyl-2,3-dihydro-1,4-oxathiine-5-carbonyl)amino]benzoate
https://huagongshe.com/reaction/326327
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acid | HCID 539946 | — |
| 反応物 | Propan-2-yl 5-amino-2-chloro-4-fluorobenzoate | HCID 13519894 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Isopropyl 2-chloro-4-fluoro-5-[(6-methyl-2,3-dihydro-1,4-oxathiine-5-carbonyl)amino]benzoate | HCID 465792 | — |
反応手順
Thionyl chloride (4.2 g, 0.035 mole) was added to a stirring slurry of 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxylic acid 4.8 g, 0.030 mole) in methylene chloride (40 ml). The mixture was warmed to 35° C. for 3 hours, then left stirring overnight at room temperature. The solution was then evaporated under reduced pressure at about 35° C. The solid residue, crude 5,6-dihydro-2-methyl-1,4-oxathiin-3-carbonyl chloride, was dissolved in methylene chloride (50 ml) and the solution chilled in ice and treated dropwise with a solution of 1-methylethyl 5-amino-2-chloro-4-fluorobenzoate (7.0 g, 0.030 mole) and triethylamine (3.5 g, 0.035 mole) in methylene chloride (50 ml). The addition was carried out over 2 hours, after which the reaction mixture was stirred at 20°-35° C. for 3 hours.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05268389 |
|---|
| 出典データセット | uspto-grants-1993_12 |
|---|
| ORD ID | ord-4f33e15d5d564d7dbd87625f99acd3c0 |
|---|
| 出典メモ | uspto-grants-1993_12 |
|---|