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HRID 1765334作成日:2026年10月25日
O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate → 2-{[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino}ethane-1-sulfonic acid
https://huagongshe.com/reaction/1765334
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| 反応物 | Tetrabutylammonium taurine | HCID 21896665 | — |
| 反応物 | N-Boc-p-hydroxyphenylglycine | HCID 21896684 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-{[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino}ethane-1-sulfonic acid | HCID 71363085 | — |
反応手順
N-Boc-4-hydroxyphenylglycine (1.00 g, 3.21 mmol) was dissolved in DMF (5 ml) and tetrabutylammonium taurine (2.36 g, 6.42 mmol) was added together with additionally 5 ml DMF. The resulting suspension was cooled on ice and TBTU (1.24 g, 3.85 mmol) was added. The ice bath was removed after 30 min and the mixture was stirred for 2 hours before it was filtered and concentrated. TFA in DCM (20%, 20 ml) was added and the reaction mixture was stirred over night. Ethanol (20 ml) was added and the solvents evaporated. The crude product was refluxed in ethanol (100 ml) for 1 hour. Filtration yielded the pure title compound as a white solid, 626 mg (71%). NMR DMSO-d6): 2.4–2.6 (m, 2H),3.2–3.4 (m, 2H),4.79 (s, 1H), 6.78 (d, 2H), 7.23 (d, 2H), 8.22 (t, 1H), 8.4 (brs, 3H), 9.7 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07226943B2 |
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| 出典データセット | uspto-grants-2007_06 |
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| ORD ID | ord-dd0441e2f89c4612b064616c35b4eae4 |
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| 出典メモ | uspto-grants-2007_06 |
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