化工社化工社 化学情報印刷レポート · 研究参考用
4-Amino-6-chlorotoluene-2-sulphonic acid → O-{[(3-chloro-4-methyl-5-sulfophenyl)amino]carbonyl}-L-serine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Amino-6-chlorotoluene-2-sulphonic acid | HCID 80805 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Triphosgene | HCID 94429 | — |
| 反応物 | Boc-Ser-Otbu | HCID 7019054 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | O-{[(3-chloro-4-methyl-5-sulfophenyl)amino]carbonyl}-L-serine | HCID 45275789 | — |
反応手順
Boc-Ser-OtBu, 100 mg (0.38 mmol), 86 mg (0.38 mmol) of 5-amino-3-chloro-2-methylbenzenesulfonic acid and 37 mg (0.0127 mmol) of triphosgene were suspended in 1 ml of methylene chloride, and 66 μl (0.76 mmol) of DIEA was added to the suspension. After stirring at room temperature overnight, the solvent was removed by distillation. The mixture was purified according to the purification step A to give the protected title compound. The resulting protected product was dissolved in 2 ml of trifluoroacetic acid and stirred for 2 hours. The solvent was removed by distillation and the mixture was purified according to the purification step A to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09000208B2 |
| 出典データセット | uspto-grants-2015_04 |
| ORD ID | ord-635790240b2649adaeaf4ce29fb1e702 |
| 出典メモ | uspto-grants-2015_04 |