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HRID 131372생성일: 2026년 10월 26일

2-Nitro-benzo[B]thiophene-3-carbonitrile → 2-Amino-1-benzothiophene-3-carbonitrile

https://huagongshe.com/reaction/131372

반응식

참여 물질

역할이름HCID투입량
반응물2-Nitro-benzo[B]thiophene-3-carbonitrileHCID 21093509—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매1,2-DichloroethaneHCID 11—
생성물2-Amino-1-benzothiophene-3-carbonitrileHCID 2327358173%

반응 단계

Combine in a 500 mL schlenk flask, 2-nitro-benzo[b]thiophene-3-carbonitrile (5.8 g, 28.4 mmol) and Pd/C (3.0 g, 10% w/w, 2.84 mmol) in 1,2-dichloroethane (120 ml), the reaction mixture is charged with a balloon of hydrogen. After overnight stirring, release the hydrogen, remove the catalyst by filtration, and wash the catalyst by 1,2-dichloroethane several times. Concentrate down to a residue, which purified by flash chromatography on silica gel, gradient (100% hexane to 100% of Hexane:CH2Cl2:EtOAc=50:50:2.5), afford brownish solid 3.6 g of title compound (yield 73%). Mass spectrum: ES(+)(m/e): 175(M+1); 1H NMR (300 MHz, DMSO-d6, ppm): δ 7.81 (br, 2H), 7.65-7.62 (m, 1H), 7.28-7.24 (m, 2H), 7.11-7.01 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384934B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-b157e65de4714409b6d75a3b89a73a24
출처 메모uspto-grants-2008_06