1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 52950745, 화합물

HRID 83043노트

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HRID 83043 반응식
Cl.[CH3:2]/[C:3](=[CH:10]\[CH3:11])/[CH2:4][O:5][CH:6]1[CH2:9][NH:8][CH2:7]1.CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1.C(N(C(C)C)CC)(C)C.Cl.[O:43]=[C:44]1[NH:53][C:52]2[N:51]=[CH:50][C:49](/[CH:54]=[CH:55]/[C:56](O)=[O:57])=[CH:48][C:47]=2[CH2:46][CH2:45]1>CN(C)C=O.O.C(OCC)(=O)C>[CH3:2]/[C:3](=[CH:10]\[CH3:11])/[CH2:4][O:5][CH:6]1[CH2:9][N:8]([C:56](=[O:57])/[CH:55]=[CH:54]/[C:49]2[CH:48]=[C:47]3[C:52](=[N:51][CH:50]=2)[NH:53][C:44](=[O:43])[CH2:45][CH2:46]3)[CH2:7]1

참가 물질

9

실험 절차

(E)-3-(2-Methylbut-2-enyloxy)azetidine hydrochloride (168 mg, 0.94 mmol), EDCI (182 mg, 0.94 mmol), HOBt (132 mg, 0.94 mmol) and diisopropylethylamine (276 μL, 1.58 mmol) were successively added to a solution of (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)-acrylic acid hydrochloride (161 mg, 0.63 mmol) in dimethylformamide (12 mL) at room temperature. The reaction mixture was stirred overnight then diluted by addition of ethyl acetate (40 mL) and water (40 mL). The aqueous layer was separated and extracted with ethyl acetate (2×40 mL). The combined organic phases were washed with a saturated solution of sodium chloride (3×50 mL), dried over sodium sulfate, filtered and concentrated to dryness. The residue was purified by chromatography on silica gel using dichloromethane/methanol (98:2) as eluent. After trituration in diethyl ether, petroleum ether and methanol, the title product was obtained as a white solid (46 mg, 21%).

후처리

  1. customThe aqueous layer was separated
  2. extractionextracted with ethyl acetate (2×40 mL)
  3. washThe combined organic phases were washed with a saturated solution of sodium chloride (3×50 mL)
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated to dryness
  7. customThe residue was purified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-8b7b9e4164f2444aa733a1871d24bbf0
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08846711B2

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