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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2410753생성일: 2026년 10월 26일

1,2-Dichloroethane → methyl 2-bromo-7-(4-morpholinyl)-5H-pyrido[2',3':4,5]pyrrolo[2,3-b]pyridine-4-carboxylate

https://huagongshe.com/reaction/2410753

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물Methyl 3-azido-6-bromo-6'-morpholino-2,3'-bipyridine-4-carboxylateHCID 86663023—
촉매Rhodium(II) Octanoate DimerHCID 6099591—
용매TetrahydrofuranHCID 8028—
생성물methyl 2-bromo-7-(4-morpholinyl)-5H-pyrido[2',3':4,5]pyrrolo[2,3-b]pyridine-4-carboxylateHCID 86663024745%

반응 조건

온도80 °C

반응 단계

1,2-Dichloroethane (0.4 mL) was added to a mixture of methyl 3-azido-6-bromo-6′-morpholino-2,3′-bipyridine-4-carboxylate (240 mg, 0.572 mmol), rhodium octanoate dimer (35.7 mg, 0.046 mmol) and crushed 4 A° molecular sieves (500 mg gm) and heated overnights at 80° C. The reaction was diluted with THF and filtered. The collected solid was washed with multiple portions of boiling THF to extract all of the product. The solvent was removed from the combined filtrates and the residue was suspended in MeOH and the product was collected by filtration. This left methyl 2-bromo-7-(4-morpholinyl)-5H-pyrido[2′,3′:4,5]pyrrolo[2,3-b]pyridine-4-carboxylate (167 mg, 0.427 mmol, 745% yield) as a yellow solid. 1H NMR (500 MHz, DMSO-d6) δ ppm 11.75 (1H, s), 8.30 (1H, d, J=8.85 Hz), 7.72 (1H, s), 6.91 (1H, d, J=8.85 Hz), 4.01 (3H, s), 3.74 (8H, dd, J=15.56, 4.88 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08815840B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-ae1072e84508459d90a9512f50a1bc26
출처 메모uspto-grants-2014_08