Maleic Acid → HCID 68525872, 화합물

HRID 1932547노트

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HRID 1932547 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:27]=[CH:28][C:29]=1[Cl:30])[C:5]([NH:7][C:8]1[CH:9]=[CH:10][C:11]([O:14][C:15]2C=CC(CNCC(O)=O)=[CH:17][CH:16]=2)=[N:12][CH:13]=1)=[O:6].[O:31]1[C:36]2[CH:37]=[CH:38][C:39]([CH2:41][N:42]3[CH2:47][CH2:46][NH:45][CH2:44][CH2:43]3)=[CH:40][C:35]=2[O:34][CH2:33][CH2:32]1.O.ON1C2C=CC=CC=2N=N1.Cl.C(N=C=N[CH2:65][CH2:66][CH2:67][N:68]([CH3:70])[CH3:69])C.[C:71]([OH:78])(=[O:77])/[CH:72]=[CH:73]\[C:74]([OH:76])=[O:75]>CN(C=O)C>[C:71]([OH:78])(=[O:77])/[CH:72]=[CH:73]\[C:74]([OH:76])=[O:75].[Cl:1][C:2]1[CH:3]=[C:4]([CH:27]=[CH:28][C:29]=1[Cl:30])[C:5]([NH:7][C:8]1[CH:13]=[N:12][C:11]([O:14][C:15]2[CH:65]=[CH:66][C:67]([N:68]([CH2:69][C:74]([N:45]3[CH2:46][CH2:47][N:42]([CH2:41][C:39]4[CH:38]=[CH:37][C:36]5[O:31][CH2:32][CH2:33][O:34][C:35]=5[CH:40]=4)[CH2:43][CH2:44]3)=[O:75])[CH3:70])=[CH:17][CH:16]=2)=[CH:10][CH:9]=1)=[O:6]

참가 물질

7

실험 절차

To a solution of ({4-[5-(3,4-dichlorobenzoyl-amino)pyridin-2-yloxy]phenyl}methylamino)acetic acid (2.50 g, 5.6 mmol) in DMF (55 mL) were added 1-(2,3-dihydrobenzo[1,4]dioxin-6-ylmethyl)piperazine (1.7 g, 7.3 mmol), 1-hydroxybenzotriazole monohydrate (0.86 g, 5.6 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.29 g, 6.7 mmol) under ice cooling, and the resulting solution was stirred for 30 minutes under ice cooling and for 17 hours at room temperature. This reaction solution was concentrated under reduced pressure. Water was added to the residue, and extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated sodium bicarbonate solution and brine, dried over anhydrous magnesium sulfate, and evaporated. The residue was dissolved in ethanol (30 mL). To the resulting solution was added maleic acid (0.32 g, 2.7 mmol), and this solution was left to stand. The precipitates were collected by filtration, to thereby yield 1.45 g of the title compound.

후처리

  1. concentrationThis reaction solution was concentrated under reduced pressure
  2. additionWater was added to the residue
  3. extractionextracted with ethyl acetate
  4. washThe ethyl acetate layer was washed with a saturated sodium bicarbonate solution and brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customevaporated
  7. dissolutionThe residue was dissolved in ethanol (30 mL)
  8. waitthis solution was left
  9. filtrationThe precipitates were collected by filtration

출처 및 근거

ORD 기록
ord-6e311abed25b4fec870e30460af4a165
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08188277B2

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