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N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester → 5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester | HCID 76926 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 4,5-Diamino-1-(2-hydroxyethyl)pyrazole sulfate | HCID 11673148 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole | HCID 21904515 | 80.8% |
反応手順
To a suspension of 4,5-diamino-1-(2-hydroxyethyl)pyrazole sulfuric acid salt (1.20 g) and N-[2-(tert-butoxycarbonylamino)acetoxy]succinimide (1.35 g) in methylene chloride (20 ml) was added N-ethyldiisopropylamine (2.1 ml) under ice-cooling, and the mixture was stirred at room temperature for 17 hours. The reaction mixture was washed with water (40 ml), saturated aqueous sodium hydrogen carbonate solution (40 ml) and brine (40 ml). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The oily residue was purified by column chromatography on silica gel eluting with 10% methanol/chloroform to give 5-amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole (1.20 g) as a solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07129232B2 |
| 出典データセット | uspto-grants-2006_10 |
| ORD ID | ord-52dd1d3126c343a9b2cb3cf6af9914c6 |
| 出典メモ | uspto-grants-2006_10 |