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HRID 1915972作成日:2026年10月27日
Diethylamine → 9H-fluoren-9-ylmethyl N-ethylcarbamate;methyl 2-[[1-[[(2S)-2-formamido-3-tritylsulfanylpropanoyl]amino]cyclopropanecarbonyl]amino]acetate
https://huagongshe.com/reaction/1915972
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethylamine | HCID 8021 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Fmoc-Gly-OH | HCID 93124 | — |
| 反応物 | PyBOP | HCID 2724699 | — |
| 反応物 | {(R)-2-[(S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propionylamino]-3-methyl-butyrylamino}-acetic acid methyl ester | HCID 57696983 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Acetonitrile methylene chloride | HCID 21877088 | — |
| 生成物 | 9H-fluoren-9-ylmethyl N-ethylcarbamate;methyl 2-[[1-[[(2S)-2-formamido-3-tritylsulfanylpropanoyl]amino]cyclopropanecarbonyl]amino]acetate | HCID 86653402 | 137.6% |
反応手順
To a solution of 1 (310.5 mg, 0.420 mmol) in MeCN/CH2Cl2 (10 mL/19 mL) under Ar(g) was added diethylamine (2.9 mL, 10% v/v) and the reaction mixture stirred at rt for 1 h 50 min. The solvent was removed in vacuo, the crude mixture treated with MeCN (3×20 mL) and the solvent was removed under reduced pressure. The crude amine was then dried under high vacuum for 1 h. Then to a solution of PyBOP (234.9 mg, 0.451 mmol) and FmocGly-OH (133.86 mg, 0.450 mmol) in CH2Cl2 (20 mL) was added diisopropylethylamine (0.25 mL, 1.44 mmol) under Ar(g) with stirring for 3 min. A solution of the resultant deprotected amine of 1 in MeCN (20 mL) was added, and the resulting mixture was allowed to stir at rt for 16 h. The solvent was then removed in vacuo. Purification by flash column chromatography on silica (eluant 1:99-3:97-5:95 MeOH/CH2Cl2) gave a white solid. The material was washed with 1M HCl (aq), dried (MgSO4) and concentrated in vacuo to give 2 (228.6 mg, 0.289 mmol, 68%) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08614193B2 |
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| 出典データセット | uspto-grants-2013_12 |
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| ORD ID | ord-48eb9fbe6dff47f5bc5c0937581b752b |
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| 出典メモ | uspto-grants-2013_12 |
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