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Isopropyl iodide → HCID 10278818, 화합물

HRID 131577
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HRID 131577 반응식
I[CH:2]([CH3:4])[CH3:3].C(=O)([O-])[O-].[K+].[K+].[CH3:11][C:12]1[C:16]([CH2:17][C:18]2[S:33][C:21]3[N:22]([CH2:29][CH:30]([CH3:32])[CH3:31])[C:23](=[O:28])[N:24]([CH3:27])[C:25](=[O:26])[C:20]=3[C:19]=2[C:34]([N:36]2[CH2:40][C@H:39]([OH:41])[CH2:38][O:37]2)=[O:35])=[C:15]([CH3:42])[NH:14][N:13]=1>CN(C)C=O.O>[OH:41][C@@H:39]1[CH2:38][O:37][N:36]([C:34]([C:19]2[C:20]3[C:25](=[O:26])[N:24]([CH3:27])[C:23](=[O:28])[N:22]([CH2:29][CH:30]([CH3:32])[CH3:31])[C:21]=3[S:33][C:18]=2[CH2:17][C:16]2[C:15]([CH3:42])=[N:14][N:13]([CH:2]([CH3:4])[CH3:3])[C:12]=2[CH3:11])=[O:35])[CH2:40]1
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참가 물질

6

반응물 3

HCID 6362Isopropyl iodide2회HCID 11430Potassium Carbonate2회HCID 10226546AR-C155858

생성물 1

HCID 10278818HCID 10278818, 화합물

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

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온도
100 °C

실험 절차

2-Iodopropane (0.1 ml) and potassium carbonate (100 mg) were added to a solution of 6-[(3,5-dimethyl-1H-pyrazol-4-yl)methyl]-5-[(4S)-4-hydroxyisoxazolidin-2-ylcarbonyl]-1-(isobutyl)-3-methylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (example 11, 100 mg) in dimethylformamide (1 ml) and the mixture stirred at 100° C. After 2 hours, further 2-iodopropane (0.2 ml) and potassium carbonate (200 mg) were added. After a further 16 hours, the mixture was cooled to room temperature, diluted with water (20 ml) and extracted with ethyl acetate (2×20 ml). Combined organic extracts were treated with pyrrolidine (0.1 ml) and after 1 hour were dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure. The residue was purified by reverse-phase HPLC with gradient 0.1% aqueous ammonium acetate/acetonitrile elution to give the title compound (58 mg) as a foam. MS (APCI) 504 [M+H]+. δ 1HDMSO 0.87 (6H, d), 1.31 (6H, d), 1.99-2.14 (7H, m), 3.19-3.21 (3H, m), 3.45-4.13 (8H, m), 4.40 (1H, sept), 4.56-4.79 (1H, m), 5.48-5.55 (1H, m).

후처리

  1. waitAfter a further 16 hours
  2. temperaturethe mixture was cooled to room temperature
  3. extractionextracted with ethyl acetate (2×20 ml)
  4. additionCombined organic extracts were treated with pyrrolidine (0.1 ml) and after 1 hour
  5. dry with materialwere dried over anhydrous magnesium sulphate
  6. filtrationfiltered
  7. customevaporated under reduced pressure
  8. customThe residue was purified by reverse-phase HPLC with gradient 0.1% aqueous ammonium acetate/acetonitrile elution

출처 및 근거

ORD 기록
ord-591e1c05c13a4552bee8983aefcbe9b0
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07384950B2

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