Sulfoxonium, trimethyl-, iodide (1:1) → HCID 86622359, 화합물

HRID 501746노트

반응식

HRID 501746 반응식
[I-].C[S+](C)(C)=O.CC(C)([O-])C.[K+].[CH2:13]([O:20][C:21]([NH:23][C@@H:24]([CH2:37][C:38]1[CH:43]=[C:42]([Cl:44])[CH:41]=[C:40]([Cl:45])[CH:39]=1)[C:25]([O:27][C:28]1C=CC([N+]([O-])=O)=CC=1)=O)=[O:22])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C1COCC1>[Cl:44][C:42]1[CH:43]=[C:38]([CH2:37][C@H:24]([NH:23][C:21](=[O:22])[O:20][CH2:13][C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[C@H:25]2[CH2:28][O:27]2)[CH:39]=[C:40]([Cl:45])[CH:41]=1

참가 물질

5

반응물 3

HCID 74498Sulfoxonium, trimethyl-, iodide (1:1)HCID 23665647Potassium tert-butoxideHCID 68465085HCID 68465085, 화합물

생성물 1

HCID 86622359HCID 86622359, 화합물수율 116.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Step BF (4): To a mixture of trimethylsulfoxonium iodide (20.72 g, 94.2 mmol) in THF (175 mL) was added solid potassium t-butoxide (8.792 g, 78.7 mmol) and the mixture was refluxed for 3 h. The mixture was cooled to 0° C., to which a solution of (S)-4-nitrophenyl 2-(benzyloxycarbonylamino)-3-(3,5-dichlorophenyl)propanoate (15.35 g, 31.40 mmol) in THF (70 mL) was added. The mixture was brought to rt, and stirred for 16 h. Solvents were removed in vacuo. Water and EtOAc were then added, and the solid material filtered (Buchner funnel). The yellowish solid was washed with water and hexane until a white solid remained. The solid was dried in a vacuum oven. All liquid layers were combined and extracted 3 times to EtOAc. The combined organic layers were back-extracted with dilute NaOH, washed with brine, dried over MgSO4, and concentrated in vacuo. The combined material was the desired compound (13.40 g, 97% yield). 1H NMR (500 MHz, CDCl3) δ 6.99-7.39 (m, 8H) 5.80 (d, J=7.93 Hz, 1H) 5.01-5.15 (m, 2H) 4.25-4.37 (m, 2H) 3.31 (s, 3H) 3.26 (s, 3H) 2.96 (d, J=6.41 Hz, 2H).

후처리

  1. temperaturethe mixture was refluxed for 3 h
  2. additionwas added
  3. customwas brought to rt
  4. customSolvents were removed in vacuo
  5. additionWater and EtOAc were then added
  6. filtrationthe solid material filtered (Buchner funnel)
  7. washThe yellowish solid was washed with water and hexane until a white solid
  8. customThe solid was dried in a vacuum oven
  9. extractionextracted 3 times to EtOAc
  10. extractionThe combined organic layers were back-extracted with dilute NaOH
  11. washwashed with brine
  12. dry with materialdried over MgSO4
  13. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-c5c93ccc27a349ffa751b9b4a13f3b3f
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07772221B2

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