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HRID 60619作成日:2026年10月26日

Methylamine → Regadenoson

https://huagongshe.com/reaction/60619

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物2-(4-Methoxycarbonylpyrazol-1-yl)adenosineHCID 71270364—
溶媒MethanolHCID 887—
生成物RegadenosonHCID 219024—

反応条件

温度20 °C

反応手順

A suspension of 1 g of 2-(4-methoxycarbonylpyrazol-1-yl)adenosine in 10 ml of 40% methylamine in methanol is stirred in a closed flask at 20° C. until formation of a solution (3 to 5 hours). The produced solution is left to stand at the given temperature for additional 15 hours. The solution is then filtered with active charcoal and the filtrate is concentrated in vacuo. The evaporation residue, which is the amorphous form of 2-[4-[(methylamino)carbonyl]-1H-pyrazol-1-yl]adenosine, is dissolved in 2 ml of dimethylsulfoxide and left to cool down freely to room temperature. The resulting turbid solution is added to 20 ml of methanol. The separated gel-like precipitate is stirred under the boil for 1.5-2.5 hours, wherein a powder-like suspension is formed. After cooling down, sucking off, and drying, 0.8 g of 2-[4-[(methylamino)carbonyl]-1H-pyrazol-1-yl]adenosine polymorph E is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09441006B2
出典データセットuspto-grants-2016_09
ORD IDord-5bff3236154745458a05360125466024
出典メモuspto-grants-2016_09