Triethylamine → HCID 22050193, 화합물

HRID 1832011노트

반응식

HRID 1832011 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][N:12]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[CH:17]=2)[C:11](=[O:23])[C:10]=1I)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:25](N(CC)CC)[CH3:26]>C(#N)C>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][N:12]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[CH:17]=2)[C:11](=[O:23])[C:10]=1[C:25]#[CH:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

4

반응물 2

HCID 8471TriethylamineHCID 22050117HCID 22050117, 화합물

생성물 1

HCID 22050193HCID 22050193, 화합물수율 87%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Degassed a solution of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one (2.01 g, 4.62 mmol) in anhydrous acetonitrile (25 mL) under argon atmosphere. Triethylamine (1.11 g, 11 mmol) was added and quickly degassed. The reaction mixture was chilled in an ice bath for 15 minutes before adding bistriphenylphosphine-palladium chloride (0.34 g, 0.48 mmol) and cuprous iodide (0.2 g). The reaction was stirred at room temperature for 30 minutes before heating at 60° C. under an atmosphere of argon for 2 hours. The reaction mixture was filtered through a bed of celite and the filtrate was concentrated under reduced pressure. The dark brown residue was diluted with CH2Cl2 (100 mL) and washed with water. The organic extracts were combined, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The dark brown residue was purified by flash chromatography using 30% ethyl acetate in hexane. The appropriate fractions were combined and concentrated under reduced pressure to afford the desired product (1.34 g, 72%) as a light yellow solid. 1H-NMR (CD3OD, 400 MHz) δ 7.74 (d, 1H, J=7.6 Hz), 7.47 (d, 2H, J=7.6 Hz), 7.35 (m, 4H), 7.09 (m, 3H), 6.46 (d, 1H, J=7.6 Hz), 5.26 (s, 2H), 5.13 (s, 2H), 0.18 (s, 9H); ES-HRMS m/z 406.1638 (M+H calculated for C24H25NO2FSi requires 406.1610). Step 3. Preparation of 4-(benzyloxy)-3-ethynyl-1-(3-fluorobenzyl)pyridin-2(1H)-one

후처리

  1. customquickly degassed
  2. temperatureThe reaction mixture was chilled in an ice bath for 15 minutes
  3. temperaturebefore heating at 60° C. under an atmosphere of argon for 2 hours
  4. filtrationThe reaction mixture was filtered through a bed of celite
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. additionThe dark brown residue was diluted with CH2Cl2 (100 mL)
  7. washwashed with water
  8. dry with materialdried over anhydrous Na2SO4
  9. concentrationconcentrated under reduced pressure
  10. customThe dark brown residue was purified by flash chromatography
  11. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-af1ce3c62a034c8ea2ccc072c6ded6f2
출처 데이터셋
uspto-grants-2006_06
특허 번호
US07067540B2

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