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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39266생성일: 2026년 10월 23일

Alendronic Acid → HCID 87302179, 화합물

https://huagongshe.com/ko/reaction/39266

반응식

참여 물질

역할이름HCID투입량
반응물Alendronic AcidHCID 2088—
반응물DimethylformamideHCID 6228—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물Glycyl-phenylalanyl-glycineHCID 6992441—
용매Ethyl AcetateHCID 8857—
생성물HCID 87302179HCID 87302179—

반응 조건

온도0 °C

반응 단계

To a solution of bisphosphonate 8 (400 mg, 0.98 mmol) in DMF (5 mL) at 0° C. was added DIEA (341 μL, 1.96 mmol) and HBTU (372 mg, 0.98 mmol). After stirring for 10 min at 0° C., the resulting activated ester solution was added to crude tripeptide 75 (0.98 mmol) and stirring was pursued for 2.5 h at 0° C. The reaction mixture was diluted with ethyl acetate, washed with H2O, 1N HCl solution, saturated NaHCO3 solution and saturated NaCl solution. The organic layer was dried over MgSO4, filtered and concentrated to dryness. The crude product was purified by silica gel chromatography on a Biotage™ flash chromatography system using a gradient of 0-10% methanol in ethyl acetate. Compound 76 was obtained as a colorless gum (652 mg, 92%). 1H NMR (400 MHz, CDCl3) δ 1.44 (s, 9H), 2.22-2.37 (m, 2H), 2.57 (t, J=6.4 Hz, 2H), 2.62 (tt, J=23.9, 7.0 Hz, 1H), 3.03-3.09 (m, 1H), 3.14-3.20 (m, 1H), 3.77-3.93 (m, 4H), 4.58-4.63 (m, 8H), 4.66-4.71 (m, 1H), 5.21-5.26 (m, 4H), 5.33-5.41 (m, 4H), 5.89-5.99 (m, 4H), 6.58-6.66 (m, 2H), 7.09 (d, J=8.2, 1H), 7.19-7.23 (m, 3H), 7.27-7.30 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524691B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ff1ade8889734ef28619030a99ed52be
출처 메모uspto-grants-2013_09