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HRID 527030作成日:2026年10月27日

Water → (1R,3S)-3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexanecarboxylic acid

https://huagongshe.com/reaction/527030

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Lithium HydroxideHCID 3939—
反応物(1R,3S)-methyl 3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexanecarboxylateHCID 68007744—
溶媒MethanolHCID 887—
生成物(1R,3S)-3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexanecarboxylic acidHCID 68007671—

反応手順

To a solution of (1R,3S)-methyl 3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexanecarboxylate, 52j, (0.035 g, 0.083 mmol) dissolved in MeOH (5 mL) and water (1 mL) was added LiOH (0.004 g, 0.168 mmol). The reaction was allowed to stir for 2 days at room temperature and then concentrated to dryness. The residue was washed with ethanol. The combined ethanol washings were concentrated in vacuo, yielding 30 mg of desired product as an off white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09345708B2
出典データセットuspto-grants-2016_05
ORD IDord-472a56229a8146029ca864845a441587
出典メモuspto-grants-2016_05