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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

反応式

関与物質

役割名称HCID仕込み量
反応物2-MorpholinoethylamineHCID 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-diolHCID 56619484—
溶媒Dimethyl SulfoxideHCID 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 formateHCID 70020248—

反応条件

温度80 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610665B1
出典データセットuspto-grants-2003_08
ORD IDord-ca2a87c4fd9242a1a3b74f18308463b0
出典メモuspto-grants-2003_08