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Cesium carbonate → (3-Fluoro-[2,4]bipyridinyl-3'-yl)-methyl-amine

HRID 878049
ノート
印刷プレビュー

反応式

HRID 878049 の反応式
C[N:2]([C:19]1[CH:20]=[N:21][CH:22]=[CH:23][C:24]=1N1CCCCC1C)[C:3](=O)C1C=C(C(F)(F)F)C=C(C(F)(F)F)C=1.[F:32][C:33]1[C:34](B2OC(C)(C)C(C)(C)O2)=[N:35][CH:36]=[CH:37][CH:38]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C.CC([O-])=O.CC([O-])=O.[Pd+2].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.[Fe+2].Cl[Cu]>[F:32][C:33]1[C:34]([C:24]2[CH:23]=[CH:22][N:21]=[CH:20][C:19]=2[NH:2][CH3:3])=[N:35][CH:36]=[CH:37][CH:38]=1
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

8

反応物 3

HCID 10796Cesium carbonateHCID 177504653-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 86670691N-Methyl-N-(2-methyl-3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-3'-yl)-3,5-bis-trifluoromethyl-benzamide2 回

生成物 1

HCID 68294041(3-Fluoro-[2,4]bipyridinyl-3'-yl)-methyl-amine収率 92.2%

試薬・触媒・溶媒 4

HCID 62652
Cuprous chloride
触媒
HCID 167845palladium(II) acetate触媒
HCID 635956Ferrocene-1,1'-bis-(diphenylphosphine)触媒
HCID 6228Dimethylformamide溶媒

反応条件

温度
100 °C

実験手順

To a solution of compound (4-bromo-pyridin-3-yl)-methyl-amine (50 mg, 0.267 mmol, example 25, intermediate b) and 3-fluoro pyridine-2-boronic acid pinacol ester (Milestone Pharmtech LLC) (89.4 mg 0.4 mmol) dissolved in dry DMF (3 mL) in a sealed tube was added cesium carbonate (348.4 mg, 1.07 mmol) and the reaction mixture was purged with argon for 10 min. Then Pd(OAc)2 (9.38 mg, 0.013 mmol), dppf (1.48 mg, 0.0026 mmol) and CuCl (26.46 mg, 0.27 mmol) were added to the reaction mixture and again purged with nitrogen for 15 min. The reaction mixture was heated at 100° C. for 16 hours. The reaction mixture was cooled to 25° C., filtered through a bed of celite and washed with EtOAc. The organic layer was washed with water, dried over sodium sulphate and evaporated to yield the desired compound as a light yellow solid (50 mg, 92%) which was used in next step without further purification. MS (ESI): m/z=204.2 [M+H]+.

後処理

  1. customthe reaction mixture was purged with argon for 10 min
  2. customagain purged with nitrogen for 15 min
  3. temperatureThe reaction mixture was cooled to 25° C.
  4. filtrationfiltered through a bed of celite
  5. washwashed with EtOAc
  6. washThe organic layer was washed with water
  7. dry with materialdried over sodium sulphate
  8. customevaporated

出典と根拠

ORDレコード
ord-14eb9e5da0274903844a74c9025557eb
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987307B2

反応ノート

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