Diisopropylethylamine → 5-Fluoro-2-(2-isopropoxy-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester

HRID 1047749노트

반응식

HRID 1047749 반응식
[CH:1]([O:4][C:5]1[C:13]([CH3:14])=[CH:12][CH:11]=[CH:10][C:6]=1[C:7]([OH:9])=O)([CH3:3])[CH3:2].[CH2:15]([O:17][C:18]([C:20]1([NH2:30])[CH2:28][C:27]2[C:22](=[CH:23][CH:24]=[C:25]([F:29])[CH:26]=2)[CH2:21]1)=[O:19])[CH3:16].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CN(C=O)C>[CH2:15]([O:17][C:18]([C:20]1([NH:30][C:7](=[O:9])[C:6]2[CH:10]=[CH:11][CH:12]=[C:13]([CH3:14])[C:5]=2[O:4][CH:1]([CH3:2])[CH3:3])[CH2:28][C:27]2[C:22](=[CH:23][CH:24]=[C:25]([F:29])[CH:26]=2)[CH2:21]1)=[O:19])[CH3:16]

참가 물질

6

실험 절차

To a solution of 2-isopropoxy-3-methyl-benzoic acid (400 mg, 2.06 mmol), 2-amino-5-fluoro-indan-2-carboxylic acid ethyl ester (554 mg, 2.47 mmol), HATU 1.17 g, 3.09 mmol) in anhydrous DMF (10 mL) is added DIPEA (511 μL, 3.09 mmol). The resulting solution is stirred at RT overnight. After the removal of DMF in vacuo, the residue is dissolved in EtOAc (100 mL) and washed with water (1×10 mL) and brine (2×10 mL). The organic layer is dried over anhydrous Na2SO4 and concentrated in vacuo. The residue is purified by flash column chromatography (120 g silica gel, gradient elution: 5%-50% EtOAc in heptane) to give a pure product (96) as white solid (709 mg, 86%).

후처리

  1. customAfter the removal of DMF in vacuo
  2. dissolutionthe residue is dissolved in EtOAc (100 mL)
  3. washwashed with water (1×10 mL) and brine (2×10 mL)
  4. dry with materialThe organic layer is dried over anhydrous Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe residue is purified by flash column chromatography (120 g silica gel, gradient elution: 5%-50% EtOAc in heptane)

출처 및 근거

ORD 기록
ord-af522f4e73754405aa2b52a047e1edb0
출처 데이터셋
uspto-grants-2013_10
특허 번호
US08569535B2

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