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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dichloroethane | HCID 11 | — |
| 반응물 | Methyl 3-azido-6-bromo-6'-morpholino-2,3'-bipyridine-4-carboxylate | HCID 86663023 | — |
| 촉매 | Rhodium(II) Octanoate Dimer | HCID 6099591 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | methyl 2-bromo-7-(4-morpholinyl)-5H-pyrido[2',3':4,5]pyrrolo[2,3-b]pyridine-4-carboxylate | HCID 86663024 | 745% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08815840B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_08 |
|---|
| ORD ID | ord-ae1072e84508459d90a9512f50a1bc26 |
|---|
| 출처 메모 | uspto-grants-2014_08 |
|---|