4-Methylmorpholine → Methyl 4-{[3-(1,3-benzodioxol-5-yl)propanoyl]amino}benzoate

HRID 642168

반응식

HRID 642168 반응식
[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([CH2:10][CH2:11][C:12]([OH:14])=O)=[CH:4][C:3]=2[O:2]1.CN1CCOCC1.C(OC(Cl)=O)C(C)C.[NH2:30][C:31]1[CH:40]=[CH:39][C:34]([C:35]([O:37][CH3:38])=[O:36])=[CH:33][CH:32]=1>C1COCC1.CCOCC>[O:9]1[C:8]2[CH:7]=[CH:6][C:5]([CH2:10][CH2:11][C:12]([NH:30][C:31]3[CH:32]=[CH:33][C:34]([C:35]([O:37][CH3:38])=[O:36])=[CH:39][CH:40]=3)=[O:14])=[CH:4][C:3]=2[O:2][CH2:1]1

참가 물질

7

반응물 4

HCID 79724-MethylmorpholineHCID 12082Methyl 4-aminobenzoateHCID 62365Isobutyl chloroformateHCID 648103-(Benzodioxol-5-yl)propionic acid

생성물 1

HCID 9945244Methyl 4-{[3-(1,3-benzodioxol-5-yl)propanoyl]amino}benzoate수율 62%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of 3-(3,4methylenedioxyphenyl)-propionic acid (501 mg, 2.58 mmol) in anhydrous THF (10 mL) were added N-methylmorpholine (0.28 mL, 2.58 mmol) and isobutylchloroformate (0.33 mL, 2.58 mmol) at 0° C. After 30 min, at 0° C., a solution of methyl 4-aminobenzoate (390 mg, 2.58 mmol) in anhydrous THF (2 mL) was added to the reaction mixture. After 30 min the temperature was allowed to warm up to rt and stir for 24 hrs. After extraction with EtOAc (100 mL), washing with HCl (0.1 N, 50 mL) and a saturated aqueous solution of NaHCO3 (50 mL), the organic layer was dryed over sodium sulfate and evaporated under vacuo to give a solid. The residue was taken up in Et2O, filtrated and washed with Et2O gave the title compound as a white solid (62%) in a 99.4% purity by HPLC (MaxPlot detection between 230 and 400 nm).

후처리

  1. waitAfter 30 min the temperature was allowed
  2. extractionAfter extraction with EtOAc (100 mL)
  3. washwashing with HCl (0.1 N, 50 mL)
  4. customevaporated under vacuo
  5. customto give a solid
  6. filtrationfiltrated
  7. washwashed with Et2O

출처 및 근거

ORD 기록
ord-ddb53d2a52ed48cc9e35821af7aef62d
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07696231B2

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