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4-Chloro-6-methoxy-7-(3-(piperidin-1-YL)propoxy)quinazoline → HCID 10229547, 화합물

HRID 1371484
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HRID 1371484 반응식
C[Si](C)(C)N[Si](C)(C)C.[Na].[Br:11][C:12]1[C:17]([NH2:18])=[C:16]2[O:19][CH2:20][O:21][C:15]2=[CH:14][CH:13]=1.Cl[C:23]1[C:32]2[C:27](=[CH:28][C:29]([O:35][CH2:36][CH2:37][CH2:38][N:39]3[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40]3)=[C:30]([O:33][CH3:34])[CH:31]=2)[N:26]=[CH:25][N:24]=1>CN(C=O)C.O>[Br:11][C:12]1[C:17]([NH:18][C:23]2[C:32]3[C:27](=[CH:28][C:29]([O:35][CH2:36][CH2:37][CH2:38][N:39]4[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40]4)=[C:30]([O:33][CH3:34])[CH:31]=3)[N:26]=[CH:25][N:24]=2)=[C:16]2[O:19][CH2:20][O:21][C:15]2=[CH:14][CH:13]=1
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참가 물질

6

반응물 3

HCID 110021914-Chloro-6-methoxy-7-(3-(piperidin-1-YL)propoxy)quinazolineHCID 219360135-Bromo-1,3-benzodioxol-4-amineHCID 45051731Sodium hexamethyidisilazane

생성물 1

HCID 10229547HCID 10229547, 화합물수율 29.3%

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매
2회

실험 절차

Sodium hexamethyldisilazane (1M solution in THF; 0.626 ml) was added to a solution of 6-bromo-2,3-methylenedioxyaniline (0.135 g) in DMF (2 ml) and the mixture was stirred at ambient temperature for 30 minutes. A solution of 4-chloro-6-methoxy-7-(3-piperidinopropoxy)quinazoline (0.1 g) in DMF (3.5 ml) was added and the resultant mixture was stirred at ambient temperature for 3 hours. The reaction mixture was diluted with water and extracted with ethyl acetate (2×). The organic phase was washed with water and with brine, dried over magnesium sulphate and evaporated. The residue was purified by column chromatography on silica using an 80:17:3 mixture of methylene chloride, methanol and a saturated methanolic ammonia solution as eluent. There was thus obtained the title compound as a solid (0.045 g); NMR Spectrum: (DMSOd6 and CF3CO2D) 1.4 (m, 1H), 1.7 (m, 3H), 1.85 (m, 2H]), 2.3 (m, 2H), 2.95 (m, 2H), 3.25 (m, 2H), 3.55 (m, 2H), 4.05 (s, 3H), 4.3 (m, 2H), 6.15 (s, 2H), 7.05 (d, 1H), 7.3 (d, 1H), 7.4 (s, 1H), 8.15 (s, 1H), 8.9 (s, 1H); Mass Spectrum: M+H+ 515 and 517; Elemental Analysis: Found C, 55.74; H, 5.30; N, 10.76. C24H27BrN4O4 requires C, 55.93; H, 5.28; N, 10.87%.

후처리

  1. extractionextracted with ethyl acetate (2×)
  2. washThe organic phase was washed with water and with brine
  3. dry with materialdried over magnesium sulphate
  4. customevaporated
  5. customThe residue was purified by column chromatography on silica using
  6. additionan 80:17:3 mixture of methylene chloride, methanol

출처 및 근거

ORD 기록
ord-f1ad40cd42fe491b82201c54203cd3a9
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07157467B2

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