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HRID 1672245作成日:2026年10月26日
Diethyl N-(4-aminobenzoyl)-L-glutamate → 2-[4-(Pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester
https://huagongshe.com/reaction/1672245
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl N-(4-aminobenzoyl)-L-glutamate | HCID 73002 | — |
| 反応物 | 2-Chloropyrimidine | HCID 74404 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-[4-(Pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester | HCID 67334207 | 69.4% |
反応手順
2-Chloropyrimidine (0.72 g, 6.3 mmol) and N-(4-aminobenzoyl)-L-glutamic acid diethyl ester (2.04 g, 6.3 mmol, 1 equiv.) were dissolved in DMF (4 mL) and the resulting mixture was heated to 110° C. for 3 hrs. Reaction was complete as determined by TLC. The mixture was cooled to room temperature and partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSO4, and concentrated by rotavap. The residue was purified by column chromatography (silica gel, 50% EtOAc/hexane) to afford 1.75 g of desired product 2-[4-(pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester in 69% yield. MS (ESI) m/z 399.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07998965B2 |
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| 出典データセット | uspto-grants-2011_08 |
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| ORD ID | ord-a3f651a449a84e309ce94b47b31d67f3 |
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| 出典メモ | uspto-grants-2011_08 |
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