Morpholine → 6-Morpholin-4-ylimidazo[1,2-a]pyridine

HRID 616노트

반응식

HRID 616 반응식
Brc1ccc2nccn2c1.C1COCCN1>C1COCCO1.CC(C)Oc1cccc(OC(C)C)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1.Nc1ccccc1-c1ccccc1.O=C([O-])[O-].[Cl][Pd+].[Cs+].[Cs+]>c1cn2cc(N3CCOCC3)ccc2n1

참가 물질

7

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온도
90 °C

실험 절차

6-bromoimidazo[1,2-a]pyridine (299 mg, 1.52 mmol), dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine (35.4 mg, 0.08 mmol), RuPhos 2nd generation (58.9 mg, 0.08 mmol), morpholine (0.159 ml, 1.82 mmol) and cesium carbonate (1483 mg, 4.55 mmol) were dissolved in degassed 1,4-dioxane (15.100 ml). Reaction mixture was purged with nitrogen for 2-3 minutes before heating to 90 °C and stirred under nitrogen overnight. The reaction was incomplete, therefore additional morpholine (0.159 ml, 1.82 mmol), RuPhos 2nd generation (58.9 mg, 0.08 mmol) and dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine (35.4 mg, 0.08 mmol) were added and the reaction mixture washeated for a further 6.5 hours at 105°C. The reaction was still only ~20% complete therefore additional morpholine (0.318 ml), RuPhos 2nd generation (117.8 mg) and dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine (70.8 mg) were added and the reaction heated for a further 24 hours at 105°C and then allowed to cool to RT. The residue partitioned between EtOAc and water, the organic phase was separated and the aq. rextracted with more EtOAc. The combined organic extracts were washed with brine, dried over magnesium sulfate filtered and evaporated. The crude material was purified by flash silica (12g, grace) chromatography, elution gradient 0 to 10% MeOH in DCM. Pure fractions were evaporated to dryness to afford 4-(imidazo[1,2-a]pyridin-6-yl)morpholine (98 mg, 31.8 %) as a white solid.

출처 및 근거

ORD 기록
ord-c4c5eb3c12504ceeb83c5886c7e20d94
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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