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Cesium carbonate → 5-(6-(2,4-Difluorophenyl)imidazo[2,1-b]oxazol-5-yl)-3-isopropylbenzo[d]isoxazole

HRID 1711791
ノート
印刷プレビュー

反応式

HRID 1711791 の反応式
Br[C:2]1[CH:3]=[CH:4][C:5]2[O:9][N:8]=[C:7]([CH:10]([CH3:12])[CH3:11])[C:6]=2[CH:13]=1.B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)O1.C([O-])(=O)C.[K+].C(=O)([O-])[O-].[Cs+].[Cs+].[F:43][C:44]1[CH:49]=[C:48]([F:50])[CH:47]=[CH:46][C:45]=1[C:51]1[N:52]=[C:53]2[N:57]([C:58]=1I)[CH:56]=[CH:55][O:54]2>CN(C=O)C.O1CCOCC1.O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[F:43][C:44]1[CH:49]=[C:48]([F:50])[CH:47]=[CH:46][C:45]=1[C:51]1[N:52]=[C:53]2[N:57]([C:58]=1[C:2]1[CH:3]=[CH:4][C:5]3[O:9][N:8]=[C:7]([CH:10]([CH3:12])[CH3:11])[C:6]=3[CH:13]=1)[CH:56]=[CH:55][O:54]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

11

反応物 5

HCID 10796Cesium carbonateHCID 517044Potassium AcetateHCID 2733548Bis(pinacolato)diboraneHCID 594578066-(2,4-Difluorophenyl)-5-iodoimidazo[2,1-b]oxazoleHCID 594578545-Bromo-3-isopropylbenzo[d]isoxazole

生成物 1

HCID 594578075-(6-(2,4-Difluorophenyl)imidazo[2,1-b]oxazol-5-yl)-3-isopropylbenzo[d]isoxazole
収率 6.33%

試薬・触媒・溶媒 5

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)触媒HCID 178418476HCID 178418476、化合物触媒HCID 962Water溶媒HCID 6228Dimethylformamide溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
90 °C

実験手順

5-Bromo-3-isopropylbenzo[d]isoxazole (0.120 g, 0.500 mmol), bis(pinacolato)diboron (0.130 g, 0.512 mmol), potassium acetate (0.098 g, 0.99 mmol) and PdCl2(dppf) (0.033 g, 0.045 mmol) in DMF (3 mL) was heated to about 90° C. for about 2 h then cooled, evaporated, triturated with DCM then filtered. The filtrate was concentrated under reduced pressure to give a dark oil which was dissolved in 1,4-dioxane (3 mL) and water (0.5 mL). Cesium carbonate (0.405 g, 1.24 mmol), PdCl2(PPh3)2 (0.035 g, 0.050 mmol) and 6-(2,4-difluorophenyl)-5-iodoimidazo[2,1-b]oxazole (0.173 g, 0.500 mmol; Example #2, step A) were added and the mixture was heated to about 90° C. oil bath for about 16 h. The solvents were evaporated and the material was purified by reverse phase chromatography (Table 1, Method c). Evaporation of the fractions with the desired product resulted in a precipitate which was collected by filtration to give the title compound (0.012 g, 6.33% yield) as a tan solid: LC/MS (Table 1, Method a) Rt, =3.08 min; MS m/z: 380.1 (M+H)+.

後処理

  1. temperaturethen cooled
  2. customevaporated
  3. customtriturated with DCM
  4. filtrationthen filtered
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. customto give a dark oil which
  7. customThe solvents were evaporated
  8. customthe material was purified by reverse phase chromatography (Table 1, Method c)
  9. customEvaporation of the fractions with the desired product
  10. customresulted in a precipitate which
  11. filtrationwas collected by filtration

出典と根拠

ORDレコード
ord-fc3ad397889f4a128ea303c822a2f245
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07790741B2

反応ノート

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