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Diisopropylethylamine → 4H-Pyrido[1,2-a]pyrimidin-4-one

HRID 405958
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인쇄 미리보기

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HRID 405958 반응식
BrC1N=CN=C2C=1NC=N2.NC[C:13]1[N:14]=[C:15]2[CH:30]=[CH:29][CH:28]=[C:27](C)[N:16]2[C:17](=[O:26])[C:18]=1C1C=CC=C(F)C=1.CCN(C(C)C)C(C)C>C(O)CCC>[N:14]1[CH:13]=[CH:18][C:17](=[O:26])[N:16]2[CH:27]=[CH:28][CH:29]=[CH:30][C:15]=12
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참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 5287830Purine, 6-bromo-HCID 66831387HCID 66831387, 화합물

생성물 1

HCID 3547854H-Pyrido[1,2-a]pyrimidin-4-one

시약·촉매·용매 1

HCID 2631-Butanol용매

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온도
110 °C

실험 절차

A mixture of 6-bromopurine (0.02040 g, 0.1025 mmol), 2-(aminomethyl)-3-(3-fluorophenyl)-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-one (0.02420 g, 0.08542 mmol), and DIEA (0.04464 mL, 0.2563 mmol) in 1-butanol (2.000 mL) was stirred at 110° C. After 18 h, the mixture was removed from the heat and concd under reduced pressure. The crude mixture was purified by revered-phase semi-prep HPLC using 20-70% gradient of CH3CN (0.1% of TFA) in water (0.1% of TFA) over 40 min as eluent. The acetonitrile was concd under reduced pressure and to the remaining acidic aq layer was added satd NaHCO3 to neutralize the TFA salt. The resulting precipitate was collected by filtration and washed with water to give 3-(3-fluorophenyl)-6-methyl-249H-purin-6-ylamino)methyl)-4H-pyrido[1,2-a]pyrimidin-4-one as a light yellow solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 12.87 (1 H, s), 8.07-8.16 (2 H, m), 7.68 (1 H, dd, J=9.0, 7.0 Hz), 7.55 (1 H, s), 7.39-7.51 (2 H, m), 7.24-7.31 (2 H, m), 7.15-7.23 (1 H, m), 6.92-7.00 (1 H, m), 4.51 (2 H, br. s.), 2.92 (3 H, s); Mass Spectrum (ESI) m/e=402.1 (M+1).

후처리

  1. customthe mixture was removed from the
  2. temperatureheat
  3. customThe crude mixture was purified by revered-phase semi-prep HPLC
  4. customover 40 min
  5. additionwas added satd NaHCO3
  6. filtrationThe resulting precipitate was collected by filtration
  7. washwashed with water

출처 및 근거

ORD 기록
ord-a462b6d650db4109a94b8beab57aa644
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08754089B2

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