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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51605생성일: 2026년 10월 23일

Acetic Acid → HCID 178508609, 화합물

https://huagongshe.com/ko/reaction/51605

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Piperidin-4-olHCID 79341—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물Protein kinase inhibitor 9HCID 22736171—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
생성물HCID 178508609HCID 178508609—
생성물HCID 178508610HCID 178508610—

반응 조건

온도80 °C

반응 단계

A mixture of 4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclohexanone (0.997 g, 2.50 mmol), 4-hydroxypiperidine (0.760 g, 7.5 mmol), sodium triacetoxyborohydride (0.689 g, 3.25 mmol), and acetic acid (0.43 mL, 7.5 mmol) in 1,2-dichloroethane (50 mL) was stirred at 80° C. under an atmosphere of nitrogen for 58 hours. The reaction mixture was cooled and water (50 mL) and sodium bicarbonate (1.35 g, 16.1 mmol) were added and the mixture was stirred for 2 hours. The organic layer was separated, dried over magnesium sulfate, filtered, and the solvent removed under reduced pressure to yield a brown solid. The cis and trans isomers were purified by flash chromatography on silica gel (1 L 5% MeOH in CH2Cl2, then 500 mL 10% MeOH in CH2Cl2, 500 mL 50:45:5 CH2Cl2:MeOH:Et3N, and 500 mL 45:45:10 CH2Cl2:MeOH:Et3N). In order to remove residual Et3N, each of the products was taken up in CH2Cl2, washed with 40 mL water, the organic portion separated, dried over magnesium sulfate, filtered, and concentrated to yield cis-1-{4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclohexyl}-4-piperidinol as a brown solid (0.185 g, 0.382 mmol) and trans-1-{4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclohexyl}-4-piperidinol as a brown solid (0.115 g, 0.237 mmol). The cis-1-{4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclohexyl}-4-piperidinol (0.185 g, 0.383 mmol) was dissolved in warm ethyl acetate (5 mL) then added to a solution of maleic acid (0.089 g, 0.765 mmol) in ethanol (5 mL). The mixture was cooled to ambient temperature and the solid was collected by filtration and dried to give cis-1-{4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclohexyl}-4-piperidinol dimaleate salt (0.202 g) as a yellow solid: 1H NMR (d6 DMSO, 400 MHz): δ H 8.61(1H, bs), 8.25(1H, s), 7.40-7.56(5H, m), 7.08-7.19(5H, m), 6.40 (2H, bs), 6.13(4H, s), 5.00-5.20(1H, m), 4.80 (1H, m), 3.03-3.95(9H, m), 2.30-2.32(2H, m), 1.63-1.99(6H, m); RP-HPLC (Delta Pak C18, 5 μm, 300 A, 15 cm; 5%-85% acetonitrile-0.1M ammonium acetate over 20 min, 1 mL/min) Rt 13.33 min. MS: MH+ 484.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713474B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-3e7e84ecdad845869bd2c5241938e10b
출처 메모uspto-grants-2004_03