4-Ethynyl-1,1'-biphenyl → HCID 66706342, 화합물

HRID 1470640

반응식

HRID 1470640 반응식
[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6](I)[C:5]=1[NH2:11].[C:13]([C:15]1[CH:20]=[CH:19][C:18]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[CH:17][CH:16]=1)#[CH:14]>C1COCC1.[Cu]I.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl>[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:14]#[C:13][C:15]2[CH:20]=[CH:19][C:18]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[CH:17][CH:16]=2)[C:5]=1[NH2:11]

참가 물질

6

반응물 2

HCID 344644-Ethynyl-1,1'-biphenylHCID 21258150methyl 2-amino-3-iodobenzoate

생성물 1

HCID 66706342HCID 66706342, 화합물수율 76.4%

시약·촉매·용매 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 6102075Dichlorobis(triphenylphosphine)palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 2-amino-3-iodo-benzoic acid methyl ester (500 mg, 1.8 mmol), 4-ethynyl-biphenyl (416 mg, 2.3 mmol) in THF (20 mL), CuI (17 mg, 0.09 mmol), bis-(triphenylphosphine)-palladium (II)-chloride (64 mg, 0.09 mmol) and TEA (0.75 mL, 5.4 mmol) were added. This mixture was stirred at room temperature for 12 h. The progress of the reaction was monitored by TLC. After completion, the reaction mass was filtered through celite, and the collected filtrate was diluted with ethyl acetate (30 mL), washed with water (2×20 mL) and the combined organic layer was separated and dried over sodium sulphate and concentrated under reduced pressure to obtain brown mass which was purified by column chromatography using 5% ethyl acetate in hexane as an eluent to obtain 450 mg of 2-amino-3-biphenyl-4-ylethynyl-benzoic acid methyl ester as a pale yellow coloured solid (76%).

후처리

  1. filtrationAfter completion, the reaction mass was filtered through celite
  2. additionthe collected filtrate was diluted with ethyl acetate (30 mL)
  3. washwashed with water (2×20 mL)
  4. customthe combined organic layer was separated
  5. dry with materialdried over sodium sulphate
  6. concentrationconcentrated under reduced pressure
  7. customto obtain brown mass which
  8. customwas purified by column chromatography

출처 및 근거

ORD 기록
ord-ec4b4a98675e4a7e8de6f7f7588ea4e5
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09006454B2

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