関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Ammonium Bicarbonate | HCID 14013 | — |
| 反応物 | o-Bis(bromomethyl)benzene | HCID 66665 | — |
| 反応物 | 1,4-Bis(bromomethyl)benzene | HCID 69335 | — |
| 反応物 | Benzene, 1,3-bis(bromomethyl)- | HCID 69373 | — |
| 反応物 | 2,6-Bis(bromomethyl)pyridine | HCID 603610 | — |
| 反応物 | trans-1,4-Dibromo-2-butene | HCID 641245 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1,2-Dibromo-3,4-dimethylbenzene | HCID 34343 | — |
反応手順
A 100 mL flask is charged with acetonitrile (12 mL) and water (24 mL) and is degassed with argon for about 5 min. Linear peptide (0.01 mmole) and 200 mM ammonium bicarbonate (6 mL) are added followed by at least one peptide (0.012 mmole) such as, but not limited to, 1,3-bis(bromomethyl) benzene, 1,2-bis(bromomethyl)benzene, 1,4-bis(bromomethyl)benzene, 2,6-bis(bromomethyl)pyridine, (E)-1,4-dibromobut-2-ene. The reaction mixture is stirred under argon at room temperature for approximately 2 hours and monitored by LC-MS. After the reaction is complete, the reaction solution is frozen and lyophilized. HPLC purification of the crude lyophilized product followed by lyophilization of fractions containing pure peptide results in the final cyclized product as a white power.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09238676B2 |
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| 出典データセット | uspto-grants-2016_01 |
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| ORD ID | ord-116fd473aadb431cb20d499af6636211 |
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| 出典メモ | uspto-grants-2016_01 |
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