1,1'-Carbonyldiimidazole → (S)-2-Benzyloxycarbonylamino-4-oxo-hexanedioic acid 6-tert-butyl ester 1-methyl ester

HRID 19307

반응식

HRID 19307 반응식
[CH3:1][O:2][C:3](=[O:20])[C@@H:4]([NH:9][C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:11])[CH2:5][C:6]([OH:8])=O.C(N1C=CN=C1)(N1C=CN=C1)=O.[C:33]([O:37][C:38](=[O:43])[CH2:39]C(O)=O)([CH3:36])([CH3:35])[CH3:34].[O-]CC.[Mg+2].[O-]CC>O1CCCC1>[CH3:1][O:2][C:3](=[O:20])[C@@H:4]([NH:9][C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:11])[CH2:5][C:6](=[O:8])[CH2:39][C:38]([O:37][C:33]([CH3:36])([CH3:35])[CH3:34])=[O:43]

참가 물질

6

반응 조건

온도
25 °C

실험 절차

In a flask under argon was placed (S)-2-benzyloxycarbonylamino-succinic acid 1-methyl ester (3.0 g, 10.67 mmol) and tetrahydrofuran (50 mL). To this mixture was added carbonyldiimidazole (1.90 g, 11.74 mmol) and the resulting mixture was stirred at 25° C. for 6 h. In a separate round bottom flask was placed malonic acid mono t-butyl ester (1.98 g, 11.74 mmol), tetrahydrofuran (30 mL) and magnesium ethoxide (685 mg, 5.87 mmol) and the resulting mixture stirred at 25° C. for 1 h and then concentrated in vacuo. The residue was taken up in tetrahydrofuran (15 mL) and added to the flask containing the succinic acid and carbonyldiimidazole mixture and stirred at 25° C. for 16 h. The mixture was concentrated in vacuo and partitioned between diethyl ether (200 mL) and a 0.5N aqueous hydrochloric acid solution (200 mL). The organic layer was washed with a saturated aqueous sodium bicarbonate solution (150 mL), dried over sodium sulfate and concentrated. Purification by flash column chromatography (silica gel 60, 230-400 mesh; 40% ethyl acetate/hexanes) afforded (S)-2-benzyloxycarbonylamino-4-oxo-hexanedioic acid 6-t-butyl ester 1-methyl ester (3.04 g, 75%) as a pale yellow oil.

후처리

  1. customIn a flask under argon was placed
  2. customIn a separate round bottom flask was placed
  3. concentrationconcentrated in vacuo
  4. additionadded to the flask
  5. additioncontaining the succinic acid and carbonyldiimidazole mixture
  6. stirringstirred at 25° C. for 16 h
  7. concentrationThe mixture was concentrated in vacuo
  8. custompartitioned between diethyl ether (200 mL)
  9. washThe organic layer was washed with a saturated aqueous sodium bicarbonate solution (150 mL)
  10. dry with materialdried over sodium sulfate
  11. concentrationconcentrated
  12. customPurification by flash column chromatography (silica gel 60, 230-400 mesh; 40% ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-df18b23ab4b4405da9bf1297fdc88c42
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07741327B2

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