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HRID 1924265作成日:2026年10月27日

Acetic Acid → 1-(1H-pyrazol-4-ylmethyl)-1,3-dihydro-2H-indol-2-one hydrate

https://huagongshe.com/reaction/1924265

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物2-Aminophenylacetic acidHCID 583776—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-tosyl-1H-pyrazole-4-carbaldehydeHCID 57743031—
溶媒WaterHCID 962—
溶媒Oxolane--water (1/1)HCID 21881883—
生成物1-(1H-pyrazol-4-ylmethyl)-1,3-dihydro-2H-indol-2-one hydrateHCID 671136058%

反応条件

温度0 °C

反応手順

In a 100 ml, three-necked flask fitted with a magnetic stirrer, 1-[(4-methylphenyl)sulfonyl]-1H-pyrazole-4-carbaldehyde x58 (1.65 g, 6.6 mmol) is dissolved in a 1/1 mixture of THF/H2O (50 ml) and the solution containing (2-aminophenyl)acetic acid x96 (1 g, 66 mmol) is added. The pH is adjusted to 5 with acetic acid and the mixture is cooled to 0° C. Sodium triacetoxyborohydride (2.10 g, 10 mmol) is added and the mixture is stirred overnight at room temperature. Water is added and the aqueous phase is extracted three times with CH2Cl2. The combined organic phases are washed with brine, dried over MgSO4 and evaporated. Purification of the residue by preparative chromatography on silicagel and recrystallization from AcOEt affords 106 mg of pure 1-(1H-pyrazol-4-ylmethyl)-1,3-dihydro-2H-indol-2-one hydrate 173.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08178533B2
出典データセットuspto-grants-2012_05
ORD IDord-a0ecb6dfa19a49b988dcfc199e8c3588
出典メモuspto-grants-2012_05