Triphenylphosphine → HCID 67505124, 화합물

HRID 1929923노트

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HRID 1929923 반응식
[C:1]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=1)#[CH:2].[CH3:9][O:10][C:11](=[O:26])[C:12]1[CH:17]=[C:16]([C:18]2[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][CH:19]=2)[C:15](Cl)=[N:14][CH:13]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O1CCCC1.C(N(C(C)C)C(C)C)C.[Cu]I>[CH3:9][O:10][C:11](=[O:26])[C:12]1[CH:17]=[C:16]([C:18]2[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][CH:19]=2)[C:15]([C:2]#[C:1][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=2)=[N:14][CH:13]=1

참가 물질

7

반응물 3

HCID 11776TriphenylphosphineHCID 137268EthynylpyridineHCID 73013037HCID 73013037, 화합물

생성물 1

HCID 67505124HCID 67505124, 화합물

시약·촉매·용매 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 8028Tetrahydrofuran용매2회HCID 81531Diisopropylethylamine용매2회

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온도
120 °C

실험 절차

A degassed solution of 2-ethynyl-pyridine (2.0 mmol, CAN 1945-84-2) in tetrahydrofuran and N-ethyldiisopropylamine (1:1, 10 ml) was added to a degassed suspension of 6-chloro-5-(4-chloro-phenyl)-nicotinic acid methyl ester (1.0 mmol), [1,1′-bis(diphenylphosphino)-ferrocene]palladium(II) dichloride dichloromethane complex (1:1) (49 mg, 0.06 mmol), polymer supported triphenylphoshine (135 mg, 1.48 mmol/g, 0.2 mmol) and copper(I)iodide (11 mg, 0.06 mmol) in tetrahydrofuran and N-ethyldiisopropylamine (1:1, 5 ml). The reaction mixture was heated at 120° C. for 20 hours under an atmosphere of nitrogen. The reaction mixture was cooled to room temperature and the solids were removed by filtration. The solids were washed with ethyl acetate (100 ml), the organic liquors were combined and washed with saturated aqueous ammonium chloride solution (3×50 ml). The organic layer was then dried over MgSO4 and concentrated in vacuo. Purification by flash column chromatography (20% ethyl acetate/heptane) gave the title compound as brown oil.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customthe solids were removed by filtration
  3. washThe solids were washed with ethyl acetate (100 ml)
  4. washwashed with saturated aqueous ammonium chloride solution (3×50 ml)
  5. dry with materialThe organic layer was then dried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customPurification by flash column chromatography (20% ethyl acetate/heptane)

출처 및 근거

ORD 기록
ord-a66700e5dc6845d99dd6923d1bd440f5
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08188093B2

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