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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252513생성일: 2026년 10월 25일

Chlorosulfonyl isocyanate → 6-methoxy-2-methyl-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/252513

반응식

참여 물질

역할이름HCID투입량
반응물Chlorosulfonyl isocyanateHCID 70918—
반응물Sodium BicarbonateHCID 516892—
반응물6-methoxy-2-methyl-1H-indoleHCID 10844709—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
생성물6-methoxy-2-methyl-1H-indole-3-carbonitrileHCID 1390464081%

반응 단계

To a solution of 6-methoxy-2-methyl-1H-indole (3.9 g, 24 mmol) in acetonitrile (200 mL) and DMF (20 mL) is added dropwise a solution of ClSO2NCO (4 mL, 1.3 eq.) in acetonitrile (31 mL) at 0° C. After the addition, the mixture is stirred at room temperature for 3 h. Then it is poured into ice water and saturated NaHCO3 is added to it until it becomes basic. The aqueous phase is extracted with CH2Cl2 and then evaporated. The residue is purified with flash column chromatography on silica gel using EtOAc/petroleum ether (1/5) as eluent to yield 81% of 6-methoxy-2-methyl-1H-indole-3-carbonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868037B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-a3b2adcd5e7a4039b8a70e9d60a9474a
출처 메모uspto-grants-2011_01