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HRID 397979作成日:2026年10月25日
2-Morpholinoethylamine → (2r,3r,4s,5s)-2-[6-(1-Ethyl-propylamino)-2-(2-morpholin-4-yl-ethylamino)-purin-9-yl]-5-(3-methyl-[1,2,4]oxadiazol-5-yl)-tetrahydro-furan-3,4-diol formate
https://huagongshe.com/reaction/397979
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2-Morpholinoethylamine | HCID 408285 | — |
| 反応物 | (2r,3r,4s,5s)-2-[2-Chloro-6-(1-ethyl-propylamino)-purin-9-yl]-5-(3-methyl-[1,2,4]oxadiazol-5-yl)-tetrahydro-furan-3,4-diol | HCID 56619484 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | (2r,3r,4s,5s)-2-[6-(1-Ethyl-propylamino)-2-(2-morpholin-4-yl-ethylamino)-purin-9-yl]-5-(3-methyl-[1,2,4]oxadiazol-5-yl)-tetrahydro-furan-3,4-diol formate | HCID 70020248 | — |
反応手順
Intermediate 11 (0.069 g, 0.163 mmol) and 4-(2-aminoethyl)morpholine (0.107 ml, 0.815 mmol) were dissolved in DMSO (0.03 ml) and heated at 80° C. for 26 h in a sealed vial (eg Reacti vial™), a further portion of 4-(2-aminoethyl)morpholine (0.053 ml, 0.407 mmol) was added after the first 20 h. The product was purified by Autoprep. HPLC to give the title compournd after freeze drying as a brown solid (0.059 g). LC/MS system B Rt=2.19 min, m/z=517MH+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06610665B1 |
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| 出典データセット | uspto-grants-2003_08 |
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| ORD ID | ord-ca2a87c4fd9242a1a3b74f18308463b0 |
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| 出典メモ | uspto-grants-2003_08 |
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