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3-Aminobenzenesulfonic acid → 3-({[(2S)-2-amino-3-methoxy-3-oxopropoxy]carbonyl}amino)benzene-1-sulfonic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Aminobenzenesulfonic acid | HCID 8474 | — |
| 反応物 | Triphosgene | HCID 94429 | — |
| 反応物 | N-Boc-L-serine methyl ester | HCID 7019177 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 3-({[(2S)-2-amino-3-methoxy-3-oxopropoxy]carbonyl}amino)benzene-1-sulfonic acid | HCID 53469025 | — |
反応手順
Boc-Ser-OME, 110 mg (0.5 mmol), and 87 mg (0.5 mmol) of 3-aminobenzenesulfonic acid were dissolved in 1 ml of pyridine, and 50 mg of triphosgene was added to the solution. The mixture was stirred at room temperature for 2 hours and the solvent was then distilled off. The resulting residue was purified according to the purification step A to give the crude product of the protected title compound. The crude product obtained was dissolved in 1 ml of methylene chloride and 1 ml of trifluoroacetic acid. The solution was stirred for 30 minutes at room temperature. After the solvent was distilled off, the mixture was purified in accordance with 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 | US08877739B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-2e7ef2063258432bad11c8aa4ee0766d |
| 出典メモ | uspto-grants-2014_11 |