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HRID 1272480作成日:2026年10月25日
Bicarbonate Ion → 2-[(2,4-Diamino-pteridin-6-ylmethyl)-amino]-3-(4-hydroxy-phenyl)-propionic Acid Tert-butyl Ester
https://huagongshe.com/reaction/1272480
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bicarbonate Ion | HCID 769 | — |
| 反応物 | Tert-butyl tyrosinate | HCID 86078 | — |
| 反応物 | 6-(Bromomethyl)-2-imino-2,3-dihydropteridin-4-amine--hydrogen bromide (1/1) | HCID 12503242 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | 2-[(2,4-Diamino-pteridin-6-ylmethyl)-amino]-3-(4-hydroxy-phenyl)-propionic Acid Tert-butyl Ester | HCID 58847294 | 71% |
反応手順
To a solution of 6-bromomethyl-2,4-pteridinediamine hydrobromide (31.2 mg, 0.116 mmol) in anhydrous N,N dimethylacetamide was added 2-amino-3-(4-hydroxy-phenyl)-propionic acid tert-butyl ester (30.22 mg, 0.127 mmol). The reaction mixture was stirred at 50° C. overnight. The crude product was poured into saturated bicarbonate solution. The resulted precipitate was collected and purified by preparative HPLC. 17.2 mg product was obtained. Yield: 71%; 1H NMR (500 MHz, DMSO-d6): δ 1.33577 (s, 9H), 2.94185–3.02295 (m, 2H), 3.6550(b, 1H), 4.0878 (s, 2H), 6.70174–6.72384 (dd, J1=8.545 Hz, J2=2.59 Hz, 2H), 7.02394–7.04103 (d, J=8.545 Hz, 2H); 9.38501 (s, 1H); ESI-MS: 412 (M++1)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07208493B2 |
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| 出典データセット | uspto-grants-2007_04 |
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| ORD ID | ord-db528565b4e64ba28567f89edb9fd6e7 |
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| 出典メモ | uspto-grants-2007_04 |
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