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3-Iodobenzyloxybenzene → 2-Methyl-1-(3-phenylmethoxyphenyl)-6-(trifluoromethoxy)indole

HRID 445
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HRID 445 반응식
Cc1cc2ccc(OC(F)(F)F)cc2[nH]1.Ic1cccc(OCc2ccccc2)c1>C1COCCO1.CC(C)(C)P(c1ccccc1-c1ccccc1)C(C)(C)C.CC(C)(C)[O-].O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.[Na+].[Pd].[Pd]>Cc1cc2ccc(OC(F)(F)F)cc2n1-c1cccc(OCc2ccccc2)c1
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참가 물질

7

반응물 2

HCID 42280193-IodobenzyloxybenzeneHCID 121806692-Methyl-6-(trifluoromethoxy)-1H-indole

생성물 1

HCID 592167202-Methyl-1-(3-phenylmethoxyphenyl)-6-(trifluoromethoxy)indole수율 40.17%

시약·촉매·용매 4

HCID 23676156Sodium t-butoxide시약HCID 27342152-(Di-tert-butylphosphino)biphenyl촉매
HCID 9811564
Bis(dibenzylideneacetone)palladium
촉매
HCID 312751,4-Dioxane용매

반응 조건

온도
120 °C

실험 절차

EN04773-50, _Buchwald coupling,_ ** _J. Med. Chem. 2009, page 3846-3854 (changed: solvent to dioxane and bromide to iodide)._** The indole from 4773-41, 1-(benzyloxy)-3-iodobenzene, Pd2(dba)3, JohnPhos and KOtBu were dissolved in toluene. The mixture was warmed at 120 °C for 1h and ~40% conversion was observed on NMR. The reaction mixture was further heated at 80 °C for 16h and 40 h, see attached 1H-NMR for reaction progress. A comparison with 4773-51 shows that using dioxane or iodide gives a lower yield (slower reaction). Switching the solvent to toluene was explored in 4773-52. The reaction in this experiment showed that the Buchwald conditions worked. Reaction mixture was thrown away.

출처 및 근거

ORD 기록
ord-232b7429c3f0450bb3d4836c8a002e13
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
출처 보기

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