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Water → HCID 11386311, 화합물

HRID 1442989
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HRID 1442989 반응식
Br[CH2:2][CH2:3][OH:4].C(=O)([O-])[O-].[K+].[K+].[Cl:11][C:12]1[CH:13]=[C:14]([CH:38]=[CH:39][C:40]=1[F:41])[NH:15][C:16]1[C:25]2[C:20](=[CH:21][C:22]([OH:37])=[CH:23][C:24]=2[O:26][CH2:27][C@H:28]2[CH2:32][CH2:31][CH2:30][N:29]2[C:33](=[O:36])[CH2:34][OH:35])[N:19]=[CH:18][N:17]=1.O>CN(C=O)C>[Cl:11][C:12]1[CH:13]=[C:14]([CH:38]=[CH:39][C:40]=1[F:41])[NH:15][C:16]1[C:25]2[C:20](=[CH:21][C:22]([O:37][CH2:2][CH2:3][OH:4])=[CH:23][C:24]=2[O:26][CH2:27][C@H:28]2[CH2:32][CH2:31][CH2:30][N:29]2[C:33](=[O:36])[CH2:34][OH:35])[N:19]=[CH:18][N:17]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 108982-BromoethanolHCID 11430Potassium CarbonateHCID 136344269HCID 136344269, 화합물

생성물 1

HCID 11386311HCID 11386311, 화합물수율 45%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
70 °C

실험 절차

2-Bromoethanol (51 μl) and potassium carbonate (86 mg) were added to a mixture of 4-[3-chloro-4-fluoroanilino]-5-{[(2R)-1-glycoloylpyrrolidin-2-yl]methoxy}-quinazolin-7-ol (70 mg) in DMF and the reaction mixture was heated at 70° C. for 16 hours. The reaction mixture was cooled to room temperature and then water (5 ml) was added to leave a white precipitate. The precipitate was filtered, washed with water and then purified by column chromatography using 2-5% methanol in DCM as eluent. The product was purified further by acidic reverse phase HPLC, and then the combined fractions were reduced to a third of the initial concentration, basified with sodium carbonate and extracted with ethyl acetate. The organic layer was dried (Na2SO4) and concentrated in vacuo to give the title compound as a white solid (35 mg, 45%); NMR Spectrum (DMSO-d6 at 373 K) 9.80 (br s, 1H), 8.40 (s, 1H), 8.15 (m, 1H), 7.65 (m, 1M, 7.33 (m, 1H), 6.80 (m, 2H), 4.60 (m, 1H), 4.50 (m, 1H), 4.30-4.10 (m, 4H), 4.0 (m, 2H), 3.75 (m, 2H), 3.60 (m, 1H), 3.50-3.37 (m, 2H), 2.10-1.85 (m, 4H); Mass spectrum MH+ 491.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customto leave a white precipitate
  3. filtrationThe precipitate was filtered
  4. washwashed with water
  5. custompurified by column chromatography
  6. customThe product was purified further by acidic reverse phase HPLC
  7. concentrationconcentration
  8. extractionextracted with ethyl acetate
  9. dry with materialThe organic layer was dried (Na2SO4)
  10. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-6d6a7785d6f34337a2d5328952772d2e
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07659279B2

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