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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272763생성일: 2026년 10월 26일

Triethylamine → 6-Azaindole

https://huagongshe.com/reaction/272763

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물7-Chloro-1H-pyrrolo[2,3-c]pyridineHCID 11435048—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물6-AzaindoleHCID 9219100%

반응 단계

A mixture of Example 695H (3.6 g, 23.6 mmol), Pd/C (0.5 g, 5%), and Et3N (2.3 g, 23.6 mmol) in MeOH (100 mL) was stirred under a balloon of hydrogen at room temperature overnight. The reaction mixture was filtered through diatomaceous earth (Celite®), and the solid was washed with additional MeOH. The solvent was removed to near dryness, and the semi-solid was treated with 300 mL of EtOAc. The precipitate was removed right away by filtration, and the filtrate was concentrated. The residue was re-dissolved in CH2Cl2, and loaded onto a silica gel column eluted with 100/5:0/5 (EtOAc/MeOH/NH4OH) to give 2.7 g (100%) of the desired product. MS (DCI) m/e 119 (M+H)+, 1H NMR (300 MHz, DMSO-d6): □ 11.6 (br s, 1H), 8.76 (dd, J=1.0, 1.0 Hz, 1H), 8.08 (d, J=5.4 Hz, 1H), 7.60 (d, J=3.0 Hz, 1H), 7.53 (dd, J=5.4, 1.0 Hz, 1H), 6.50 (dd, J=3.0, 1.0 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456169B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-c9e38123ed834fd79e4d9c1e1948bd21
출처 메모uspto-grants-2008_11