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Cesium carbonate → HCID 58188118、化合物

HRID 1845112
ノート
印刷プレビュー

反応式

HRID 1845112 の反応式
[CH:1]([B-](F)(F)F)=[CH2:2].[K+].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C([O-])([O-])=O.[Cs+].[Cs+].Br[C:34]1[CH:35]=[CH:36][C:37]([CH:40]([F:42])[F:41])=[N:38][CH:39]=1>C1COCC1.O.Cl[Pd]Cl.O>[F:41][CH:40]([F:42])[C:37]1[CH:36]=[CH:35][C:34]([CH:1]=[CH2:2])=[CH:39][N: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 4

HCID 10796Cesium carbonateHCID 11776TriphenylphosphineHCID 23679353Potassium vinyltrifluoroborateHCID 534150625-Bromo-2-(difluoromethyl)pyridine

生成物 1

HCID 58188118HCID 58188118、化合物収率 76.6%

試薬・触媒・溶媒 3

HCID 24290Palladium Chloride
触媒
HCID 962Water溶媒
HCID 21881883Oxolane--water (1/1)溶媒

反応条件

温度
80 °C

実験手順

To a stirred suspension of potassium vinyltrifluoroborate (3.32 g, 24.8 mmol), PdCl2 (0.1 g, 0.56 mmol) and PPh3 (0.45 g, 1.71 mmol) in 60 mL of THF—H2O (9:1) were added Cs2CO3 (20.2 g, 62 mmol) and 5-bromo-2-(difluoromethyl)pyridine (4.3 g, 20.7 mmol). The resulting reaction mixture was heated to 80° C. and stirred for 16 h. After completion of the reaction, the reaction mixture was cooled to room temperature, treated with water and extracted with CH2Cl2. The organic layer was dried over anhydrous Na2SO4 and the solvents were evaporated in vacuo. The residue was purified by column chromatography (SiO2, 5% Et2O/pentane) to afford the title compound (2.46 g, 75% yield). MS: 156 [M+1]+; 1H-NMR (300 MHz, CDCl3): δ 8.64 (s, 1H), 7.86 (d, 1H, J=8.3 Hz), 7.60 (d, 1H, J=8.3 Hz), 6.74 (dd, 1H, J=18, 11.2 Hz), 6.63 (t, 1H, J=55.6 Hz), 5.91 (d, 1H, J=18 Hz), 5.48 (d, 1H, J=11.2 Hz).

後処理

  1. customThe resulting reaction mixture
  2. customAfter completion of the reaction
  3. temperaturethe reaction mixture was cooled to room temperature
  4. extractionextracted with CH2Cl2
  5. dry with materialThe organic layer was dried over anhydrous Na2SO4
  6. customthe solvents were evaporated in vacuo
  7. customThe residue was purified by column chromatography (SiO2, 5% Et2O/pentane)

出典と根拠

ORDレコード
ord-f50d6c4d00384738bba4b19d79b6b6c3
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08946439B2

反応ノート

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