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HRID 1616052作成日:2026年10月25日

Diisopropylethylamine → HCID 178426298、化合物

https://huagongshe.com/reaction/1616052

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物3-Methylpicolinic acidHCID 268757—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物HCID 178507273HCID 178507273—
溶媒DimethylformamideHCID 6228—
生成物Ammonia methanolHCID 21705897—
生成物HCID 178426298HCID 17842629813.3%

反応条件

温度20 °C

反応手順

To 3-Methyl-2-pyridinecarboxylic acid (0.032 g, 0.234 mmol) in DMF (0.5 ml) was added HATU (0.089 g, 0.234 mmol) and the solution stirred for 10 min at 20° C. To this was then added a solution of 3-fluoro-6-(1H-indol-4-yl)-1H-indazol-4-amine (0.052 g, 0.195 mmol) in DMF (0.5 ml), followed by DIPEA (0.068 ml, 0.391 mmol) and the top was placed on the vial which had been pierced with a needle. The mixture was stirred at 20° C. for 66 hours then loaded directly onto a dry 1 g NH2 cartridge, left for 2 hours then eluted with methanol (2.5 column vols). Upon standing for 20 hours at 20° C., a solid precipitated from the orange solution which was filtered off and dried. The solid was triturated with methanol (2×2 ml) then blown to dryness and loaded onto a 500 mg SCX pre-rinsed with methanol. Elution with methanol (3 column vols) then 2M NH3/MeOH (3 column vols) and concentration of the basic fractions by blow down afforded the title compound (6 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08765743B2
出典データセットuspto-grants-2014_07
ORD IDord-fffd4132a77f4dc98301d614649637f9
出典メモuspto-grants-2014_07