Potassium Carbonate → 2-t-Butoxycarbonylamino-4-ethynyl-thiophene-3-carboxylic acid ethyl ester

HRID 1244160노트

반응식

HRID 1244160 반응식
[CH2:1]([O:3][C:4]([C:6]1[C:10]([CH:11]=O)=[CH:9][S:8][C:7]=1[NH:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])=[O:5])[CH3:2].[C:21](=O)([O-])[O-].[K+].[K+].COP(C(=[N+]=[N-])C(=O)C)(=O)OC>CCO>[CH2:1]([O:3][C:4]([C:6]1[C:10]([C:11]#[CH:21])=[CH:9][S:8][C:7]=1[NH:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])=[O:5])[CH3:2]

참가 물질

5

실험 절차

2-t-Butoxycarbonylamino-4-formyl-thiophene-3-carboxylic acid ethyl ester (6.35 g, 21.31 mmol) from example 240d was dissolved in absolute EtOH (325 mL). This was treated with potassium carbonate (%.89 g, 42.62 mmol) followed by (1-diazo-2-oxopropyl)-phosphonic acid dimethyl ester (4.91 g, 25.57 mmol). The reaction was stirred at room temperature for 14 hr. The reaction was concentrated to 12 volume then poured into sat. NaHCO3 (250 mL) and then extracted with EtOAc (3×250 mL). The combined extracts were washed with brine (2×250 mL). They were dried (Na2SO4), filtered and the solvent removed in vacuo. The crude product was purified by flash chromatography (SiO2, 1 EtOAc/9 hexanes) to afford the title compound (5.86 g, 93%). MS m/e (CI) 296.0 (M+H), 313.1 (M+NH4); 1H NMR (300 MHz, CDCl3): δ ppm 1.41 (t, 3H), 1.53 (s, 9H), 3.11 (s, 1H), 4.37 (q, 2H), 6.98 (s, 1H), 10.30 (s, 1H).

후처리

  1. concentrationThe reaction was concentrated to 12 volume
  2. additionthen poured into sat. NaHCO3 (250 mL)
  3. extractionextracted with EtOAc (3×250 mL)
  4. washThe combined extracts were washed with brine (2×250 mL)
  5. dry with materialThey were dried (Na2SO4)
  6. filtrationfiltered
  7. customthe solvent removed in vacuo
  8. customThe crude product was purified by flash chromatography (SiO2, 1 EtOAc/9 hexanes)

출처 및 근거

ORD 기록
ord-3c097bc778484801af3d008c07685cc9
출처 데이터셋
uspto-grants-2006_10
특허 번호
US07119205B2

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