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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2089043생성일: 2026년 10월 25일

4,4'-Diaminodicyclohexylmethane → N-{4-[(4-aminocyclohexyl)methyl]cyclohexyl}-6-chloro-4-(5-methoxy-1H-pyrrolo[2,3-b]pyridin-3-yl)pyridin-2-amine

https://huagongshe.com/reaction/2089043

반응식

참여 물질

역할이름HCID투입량
반응물4,4'-DiaminodicyclohexylmethaneHCID 15660—
반응물3-(2,6-Dichloro-4-pyridinyl)-5-methoxy-1H-pyrrolo[2,3-b]pyridineHCID 87192183—
용매WaterHCID 962—
생성물N-{4-[(4-aminocyclohexyl)methyl]cyclohexyl}-6-chloro-4-(5-methoxy-1H-pyrrolo[2,3-b]pyridin-3-yl)pyridin-2-amineHCID 8719106558.7%

반응 단계

A mixture of Example 149e (0.634 g, 2.16 mmol) and 4,4′-methylenedicyclohexanamine (2.267 g, 10.78 mmol) was heated at 155° C. for 90 minutes and cooled. While still warm, the slurry was treated with water and extracted with EtOAc (2×). The combined organic layers were dried over MgSO4, filtered, concentrated, and purified on a 28 g Biotage KP-NH column using the ISCO Companion flash system eluting with MeOH/EtOAc (3:97 to 5:95) to give 593 mg of the title compound. 55 mg of this material was further purified by reverse-phase HPLC as described in Example 56 to give 17 mg of the title compound as trifluoroacetic acid salts. 1H NMR (400 MHz, CD3OD) ppm 1.02-1.45 (m, 9H), 1.57-1.92 (m, 9H), 1.99-2.18 (m, 2H), 3.02 (m, 1H), 3.70 (m, 1H), 3.95 (s, 3H), 6.72-6.92 (m, 2H), 7.80-7.91 (m, 2H), 8.06 (s, 1H). MS (DCI+) m/z 468.3 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08435980B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-fee6dbc9090444cba735461608e3ab1e
출처 메모uspto-grants-2013_05