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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 513302생성일: 2026년 10월 26일

Diisopropylethylamine → 4-(2,3-Difluorobenzylamino)-6-(4-(1-(1,3-difluoropropan-2-yl)piperidin-4-yl)phenylamino)nicotinamide

https://huagongshe.com/reaction/513302

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1,3-DifluoroacetoneHCID 228397—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물4-(2,3-Difluorobenzylamino)-6-(4-(piperidin-4-yl)phenylamino)nicotinamideHCID 67500438—
용매1,2-DichloroethaneHCID 11—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물4-(2,3-Difluorobenzylamino)-6-(4-(1-(1,3-difluoropropan-2-yl)piperidin-4-yl)phenylamino)nicotinamideHCID 675021989.2%

반응 단계

Compound 4-(2,3-difluorobenzylamino)-6-(4-(piperidin-4-yl)phenylamino)nicotinamide (Example 209) (100 mg, 0.21 mmol) was stirred in 5 mL 1,2-dichloroethane and 5 mL dioxane as a slurry. To it were added DIEA (150 μL, 0.84 mmol) and then 1,3-difluoroacetone (100 mg, 1.05 mmol). The mixture was stirred at RT for 2 h. To the mixture were then added HOAc (200 μL) and NaBH(OAc)3 (222 mg, 1.05 mmol). The mixture was stirred at RT for overnight (incomplete reaction). To it was added water, and the mixture was concentrated in vacuo and subjected to reverse phase preparative HPLC to isolate the desired product (10 mg) and remaining starting compound. MS found for C27H29F4N5O as (M+H)+ 516.4. UV: λ=259 nm. 1H NMR: (CD3OD) δ 8.18 (1H, s), 7.38 (2H, d, J=8.0 Hz), 7.25 (1H, m), 7.19-7.09 (4H, m), 5.82 (1H, s), 5.15-4.90 (5H, m), 4.55 (2H, s), 3.77 (2H, m), 3.48 (2H, m), 3.03 (1H, m), 2.18 (4H, m) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102625B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-27fd9d58b687470db118f8f4ca850614
출처 메모uspto-grants-2015_08