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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1621367생성일: 2026년 10월 26일

4-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole → 1-(Oxan-2-yl)-1H-indazol-4-amine

https://huagongshe.com/reaction/1621367

반응식

참여 물질

역할이름HCID투입량
반응물4-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazoleHCID 59548298—
촉매PalladiumHCID 23938—
용매Ethyl AcetateHCID 8857—
생성물1-(Oxan-2-yl)-1H-indazol-4-amineHCID 4411823296.7%

반응 단계

A solution of 4-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (1.05 g, 4247 μmol) in EtOAc (100 mL) was treated with 10% Pd/C (60 mg) and stirred under an atmosphere of H2. The reaction was monitored by LCMS and found to be complete after 22 h. The reaction was filtered and concentrated (caution: tends to foam/bump). The residue was triturated with Et2O to give 1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-4-amine (892 mg, 96.7% yield) as an off-white solid. 1H NMR (400 MHz, d6-DMSO) δ 8.11 (s, 1H); 7.03 (t, J=7.82 Hz, 1H); 6.74 (d, J=8.22 Hz, 1H); 6.18 (d, J=7.43 Hz, 1H); 5.78 (s, 2H); 5.59-5.67 (m, 1H); 3.82-3.92 (m, 1H); 3.63-3.74 (m, 1H); 2.30-2.45 (m, 1H); 1.96-2.08 (m, 1H); 1.84-1.94 (m, 1H); 1.65-1.80 (m, 1H); 1.55 (br. s., 2H). m/z (ESI, +ve) Found 218 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08772480B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-30c048d178f14b42979588732c567a8d
출처 메모uspto-grants-2014_07