Pyridine → (S)-Benzyl 2-(2-oxooxazolidin-4-YL)acetate

HRID 1009262

反応式

HRID 1009262 の反応式
C(O[C:6]([NH:8][C@H:9]([CH2:21][OH:22])[CH2:10][C:11]([O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:12])=[O:7])(C)(C)C.N1C=CC=CC=1.C1(C)C=CC(S(OS(C2C=CC(C)=CC=2)(=O)=O)(=O)=O)=CC=1>ClC(Cl)C.ClCCl>[O:7]=[C:6]1[NH:8][C@@H:9]([CH2:10][C:11]([O:13][CH2:14][C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)=[O:12])[CH2:21][O:22]1

参加物

6

反応物 3

HCID 1049PyridineHCID 77773Toluene-p-sulphonic anhydrideHCID 10040985Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoate

生成物 1

HCID 11241814(S)-Benzyl 2-(2-oxooxazolidin-4-YL)acetate

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 63651,1-Dichloroethane溶媒

反応条件

温度
2.5 °C

実験手順

To a solution of the alcohol (95.7 g) from Step 1 in dichloroethane (925 mL) was added pyridine (625 mL) and the mixture was cooled to 0-5° C. Anhydrous p-toluenesulfonic anhydride (105.7 g) was added and the mixture was warmed to room temperature and stirred for 1 hour and then heated to 90° C. for 2 hours. The mixture was cooled, diluted with dichloromethane (1000 mL) and washed with 1N HCl (3×600 mL). The organic layer was washed with brine, dried with sodium sulfate and the solvents were removed in vacuo. The residue was purified by chromatography on SiO2 using ethyl acetate and hexanes in a 1:1 ratio followed by ethyl acetate to yield benzyl [(4S)-2-oxo-1,3-oxazolidin-4-yl]acetate.

後処理

  1. temperaturethe mixture was warmed to room temperature
  2. temperatureheated to 90° C. for 2 hours
  3. temperatureThe mixture was cooled
  4. washwashed with 1N HCl (3×600 mL)
  5. washThe organic layer was washed with brine
  6. dry with materialdried with sodium sulfate
  7. customthe solvents were removed in vacuo
  8. customThe residue was purified by chromatography on SiO2

出典と根拠

ORDレコード
ord-0a93d106bd694f2c9b327025489704d4
出典データセット
uspto-grants-2011_07
特許番号
US07973037B2

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