Pivalic acid → (R)-4-((1-cyclobutylethyl)amino)-2-(4-isopropylpyridin-2-yl)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

HRID 81086

反応式

HRID 81086 の反応式
C(P(C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2)CCC.C(O)(=O)C(C)(C)C.[F-].[Cs+].Br[C:36]1[CH:41]=[C:40]([CH:42]([CH3:44])[CH3:43])[CH:39]=[CH:38][N:37]=1.[CH:45]1([C@H:49]([NH:51][C:52]2[C:57]3[N:58]([CH2:61][C:62]4[CH:67]=[CH:66][C:65]([C:68]([F:71])([F:70])[F:69])=[CH:64][CH:63]=4)[CH:59]=[N:60][C:56]=3[C:55]([CH3:72])=[C:54]([C:73]#[N:74])[N:53]=2)[CH3:50])[CH2:48][CH2:47][CH2:46]1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O1CCOCC1>[CH:45]1([C@H:49]([NH:51][C:52]2[C:57]3[N:58]([CH2:61][C:62]4[CH:63]=[CH:64][C:65]([C:68]([F:71])([F:70])[F:69])=[CH:66][CH:67]=4)[C:59]([C:36]4[CH:41]=[C:40]([CH:42]([CH3:44])[CH3:43])[CH:39]=[CH:38][N:37]=4)=[N:60][C:56]=3[C:55]([CH3:72])=[C:54]([C:73]#[N:74])[N:53]=2)[CH3:50])[CH2:48][CH2:47][CH2:46]1

参加物

8

反応物 5

HCID 6417Pivalic acidHCID 25953Cesium fluorideHCID 11371790Bis(adamantan-1-yl)(butyl)phosphaneHCID 457879862-Bromo-4-isopropylpyridineHCID 86724464(R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

生成物 1

HCID 86724465(R)-4-((1-cyclobutylethyl)amino)-2-(4-isopropylpyridin-2-yl)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒HCID 312751,4-Dioxane溶媒2 回

反応条件

温度
70 °C

実験手順

To a vial containing palladium(II) acetate (4.3 mg, 0.019 mmol) and butyldi-1-adamantylphosphine (13.9 mg, 0.039 mmol) was added 1,4-dioxane (300 ul). The vial was evacuated and refilled with Ar (3×). The solution was warmed to 70° C. for 20 minutes. In a separate vial were combined pivalic acid (9.9 mg, 0.097 mmol), cesium fluoride (44 mg, 0.29 mmol), 2-bromo-4-isopropylpyridine (purchased from CombiPhos Catalysts, Inc.) (29 mg, 0.15 mmol), (R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile (40 mg, 0.097 mmol) and 1,4-dioxane (0.5 mL). The mixture was degassed with Ar for 15 minutes, and the catalyst solution was added to the mixture. The resulting mixture was stirred at 130° C. for 3 days. The mixture was cooled to room temperature and concentrated. The residue was dissolved in DCM and purified by silica gel chromatography (0-100% ethyl acetate/hexanes, linear gradient) to give (R)-4-((1-cyclobutylethyl)amino)-2-(4-isopropylpyridin-2-yl)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile. MS ESI calc'd for C30H31F3N6 [M+H]+ 533. found 533.

後処理

  1. customThe vial was evacuated
  2. additionrefilled with Ar (3×)
  3. customThe mixture was degassed with Ar for 15 minutes
  4. additionthe catalyst solution was added to the mixture
  5. temperatureThe mixture was cooled to room temperature
  6. concentrationconcentrated
  7. dissolutionThe residue was dissolved in DCM
  8. custompurified by silica gel chromatography (0-100% ethyl acetate/hexanes, linear gradient)

出典と根拠

ORDレコード
ord-25ba329731bc4cecab261f438551a9a2
出典データセット
uspto-grants-2014_09
特許番号
US08846657B2

関連ノート

読み込み中…