돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1445575생성일: 2026년 10월 26일

1,2-Diaminocyclohexane → [1-(4-chloro-phenyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl ester

https://huagongshe.com/reaction/1445575

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DiaminocyclohexaneHCID 4610—
반응물1-Chloro-4-iodobenzeneHCID 12510—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물methyl 2-(2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)acetateHCID 67218699—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물[1-(4-chloro-phenyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl esterHCID 67220030—

반응 조건

온도160 °C

반응 단계

A mixture of (2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-acetic acid methyl ester (100 mg, 0.49 mmol), 1-chloro-4-iodo-benzene (117 mg, 0.49 mmol), CuI (5 mg, 0.03 mmol), cyclohexane-1,2-diamine (6 μL, 0.05 mmol), potassium phosphate (218 mg, 1.0 mmol) and 1,4-dioxane (0.5 mL) is heated at 160° C. for 140 minutes. The reaction is cooled, diluted with EtOAc, filtered through silica and evaporated to dryness. The residue is purified by flash column chromatography (5:1 iso-hexane/EtOAc elution) to furnish [1-(4-chloro-phenyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl ester; MH+=315.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666878B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-9ee7b8443d4044a793a0ca295ef8bff7
출처 메모uspto-grants-2010_02