Diisopropylethylamine → HCID 86618929, 화합물

HRID 1094230노트

반응식

HRID 1094230 반응식
C(N(C(C)C)CC)(C)C.[CH:10]1([C:13]2[N:18]=[C:17]([Cl:19])[C:16]([CH3:20])=[C:15](Cl)[N:14]=2)[CH2:12][CH2:11]1.[NH:22]1[CH2:27][CH2:26][CH:25]([C:28]2[CH:37]=[CH:36][C:35]3[C:30](=[N:31][CH:32]=[CH:33][CH:34]=3)[N:29]=2)[CH2:24][CH2:23]1.N1C2C(=CC=CN=2)C=CC=1.C(=O)(O)[O-].[Na+]>O.C(OCC)(=O)C.CC(N(C)C)=O>[CH:10]1([C:13]2[N:14]=[C:15]([N:22]3[CH2:23][CH2:24][CH:25]([C:28]4[CH:37]=[CH:36][C:35]5[C:30](=[N:31][CH:32]=[CH:33][CH:34]=5)[N:29]=4)[CH2:26][CH2:27]3)[C:16]([CH3:20])=[C:17]([Cl:19])[N:18]=2)[CH2:11][CH2:12]1

참가 물질

9

반응물 5

HCID 81531DiisopropylethylamineHCID 1360691,8-NaphthyridineHCID 516892Sodium BicarbonateHCID 545957314,6-Dichloro-2-cyclopropyl-5-methylpyrimidineHCID 666409192-(Piperidin-4-YL)-1,8-naphthyridine

생성물 1

HCID 86618929HCID 86618929, 화합물수율 51.7%

시약·촉매·용매 3

HCID 962Water용매HCID 8857Ethyl Acetate용매HCID 31374Dimethylacetamide용매

반응 조건

온도
100 °C

실험 절차

20 ml of dimethylacetamide and 3.36 ml (19.2 mmoles) of diisopropylethylamine are added into a single-necked flask containing 1.5 g (7.39 mmoles) of 2-cyclopropyl-4,6-dichloro-5-methyl-pyrimidine and 1.58 g (7.39 mmoles) of 2-piperidin-4-yl-[1,8]naphthyridine. This mixture is heated at 100° C. overnight. The next day 0.2 equivalent of naphthyridine is added and the reaction mixture is heated for another 6 hours, followed by returning to ambient temperature before concentration to dryness. The residue obtained is taken up in a mixture of water, ethyl acetate and a saturated solution of sodium bicarbonate. The organic phase is separated and the aqueous phase reextracted with ethyl acetate. The collected organic phases are dried over magnesium sulphate then the solvent is evaporated off under reduced pressure (2 kPa). The residue is chromatographed on silica gel eluting with a gradient of heptane-ethyl acetate (50-50) to 100% ethyl acetate. 1.45 g of expected product is obtained.

후처리

  1. temperaturethe reaction mixture is heated for another 6 hours
  2. concentrationby returning to ambient temperature before concentration to dryness
  3. customThe residue obtained
  4. customThe organic phase is separated
  5. dry with materialThe collected organic phases are dried over magnesium sulphate
  6. customthe solvent is evaporated off under reduced pressure (2 kPa)
  7. customThe residue is chromatographed on silica gel eluting with a gradient of heptane-ethyl acetate (50-50) to 100% ethyl acetate

출처 및 근거

ORD 기록
ord-64013a6b865a4078997bd59c9f044f8b
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08133896B2

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