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HRID 1410110作成日:2026年10月23日

Diisopropylethylamine → (S)-5-chloro-N-(3-methoxy-5-(2-methylpyrrolidin-1-yl)phenyl)thiazolo[5,4-d]pyrimidin-7-amine

https://huagongshe.com/ja/reaction/1410110

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物5,7-Dichlorothiazolo(5,4-d)pyrimidineHCID 609639—
反応物(S)-3-Methoxy-5-(2-methylpyrrolidin-1-YL)anilineHCID 68379440—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物(S)-5-chloro-N-(3-methoxy-5-(2-methylpyrrolidin-1-yl)phenyl)thiazolo[5,4-d]pyrimidin-7-amineHCID 8667179277%

反応条件

温度30 °C

反応手順

The mixture of 5,7-dichlorothiazolo[5,4-d]pyrimidine (200 mg, 0.97 mmol), (S)-3-methoxy-5-(2-methylpyrrolidin-1-yl)benzenamine (220 mg, 1.07 mmol) and DIPEA (150 mg, 1.17 mmol) in DMSO (50 mL) was heated to 30° C. with stirring for 16 h. The mixture was diluted with water, extracted with ethyl acetate (50 mL), combined organics washed with water (10 mL×4) then brine (10 mL×2), dried over Na2SO4 and concentrated to give the residue which was purified by column chromatography (petroleum ether:ethyl acetate=20:1) to afford (S)-5-chloro-N-(3-methoxy-5-(2-methylpyrrolidin-1-yl)phenyl)thiazolo[5,4-d]pyrimidin-7-amine (280 mg, 77%) as yellow oil. LC-MS: 376 [M+H]+, tR=1.825 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921383B2
出典データセットuspto-grants-2014_12
ORD IDord-a9d88c5eb2e64d8387ea19e7dc7b0b4c
出典メモuspto-grants-2014_12