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HRID 16833作成日:2026年10月26日

Diisopropylethylamine → HCID 178489797、化合物

https://huagongshe.com/reaction/16833

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物(2R,6S)-1,2,6-TrimethylpiperazineHCID 30720221—
反応物2-[(2S,6R)-2,6-dimethylpiperazin-1-yl]acetonitrileHCID 86621074—
反応物HCID 178489782HCID 178489782—
溶媒Dimethyl SulfoxideHCID 679—
溶媒MethanolHCID 887—
生成物HCID 178489797HCID 17848979722%

反応手順

5-Chloro-N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]pyrazine-2-carboxamide (271 mg, 0.70 mmol) was added in one portion to a 3:1 mixture of (2R,6S)-1,2,6-trimethylpiperazine and 2-[(2S,6R)-2,6-dimethylpiperazin-1-yl]acetonitrile (180 mg, 1.40 mmol) in anhydrous dimethylsulfoxide (1.40 ml) at 25° C. The resulting solution was stirred at ambient temperature for 2 h. The reaction was incomplete and N-ethyl-N-propan-2-ylpropan-2-amine (0.24 ml, 1.40 mmol) was added and the solution was stirred at 60° C. for a further 2 h. The reaction mixture was diluted with methanol (20 mL) and purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH to afford impure material. The concentrated eluent was purified by silica column chromatography, eluting with a gradient of 0 to 5% 7M NH3/MeOH in DCM. Pure fractions were evaporated to dryness to afford the title compound (77 mg, 22%) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737149B2
出典データセットuspto-grants-2010_06
ORD IDord-6aff711b2a764f05adde870dc1799b36
出典メモuspto-grants-2010_06