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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2043625생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2043625

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-Aminophenylacetic acidHCID 583776—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-tosyl-1H-pyrazole-4-carbaldehydeHCID 57743031—
용매WaterHCID 962—
용매Oxolane--water (1/1)HCID 21881883—
생성물1-(1H-pyrazol-4-ylmethyl)-1,3-dihydro-2H-indol-2-one hydrateHCID 671136058%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08586623B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-f62d82fb9dd046bba2a1bc6dab99c2e5
출처 메모uspto-grants-2013_11