Triphenylphosphine → 3-(3-Piperidin-1-yl-propoxy)-isoxazole-5-carboxylic acid methyl ester

HRID 30484

반응식

HRID 30484 반응식
[CH3:1][O:2][C:3]([C:5]1[O:9][N:8]=[C:7]([OH:10])[CH:6]=1)=[O:4].[N:11]1([CH2:17][CH2:18][CH2:19]O)[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.N(C(OC(C)(C)C)=O)=NC(OC(C)(C)C)=O>C(Cl)Cl>[CH3:1][O:2][C:3]([C:5]1[O:9][N:8]=[C:7]([O:10][CH2:19][CH2:18][CH2:17][N:11]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)[CH:6]=1)=[O:4]

참가 물질

6

실험 절차

3-Hydroxy-isoxazole-5-carboxylic acid methyl ester (0.859 g., 6.00 mmol) and 3-piperidin-1-yl-propan-1-ol (0.860 g., 6.00 mmol) were dissolved in DCM (30 mL), and polymer-supported Ph3P resin (3 mmol/g, 3.1 g, 9.30 mmol) was added. The mixture was stirred for 10 min and di-tert-butyl azodicarboxylate (2.14 g, 9.30 mmol) was then added. The reaction mixture was stirred under nitrogen for 18 h. The reaction was quenched with 1 N NaOH (20 mL) and was stirred for 30 min. The resulting mixture was extracted with DCM (3×30 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated to yield a crude oily product (3.1 g), which was purified (SiO2: 5% 2 M NH3 in MeOH/DCM) to yield the title compound (0.88 g, 58%). MS (ESI): exact mass calcd. for C13H20N2O4, 268.14; m/z found, 269.4 [M+H]+. 1H NMR (500 MHz, CDCl3): 6.53 (s, 1H), 4.34-4.30 (m, 2H), 3.94 (s, 3H), 2.47-2.34 ( 6H), 2.02-1.94 (m, 2H), 1.61-1.54 (m, 4H), 1.47-1.39 (m, 2H).

후처리

  1. stirringThe reaction mixture was stirred under nitrogen for 18 h
  2. customThe reaction was quenched with 1 N NaOH (20 mL)
  3. stirringwas stirred for 30 min
  4. extractionThe resulting mixture was extracted with DCM (3×30 mL)
  5. dry with materialThe combined organic extracts were dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-546ba2e9a0d44059960235eb0d1660a1
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07423147B2

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