Dichloromethane → t-Butyl 5-(6-methane-sulfonyloxymethylpyridin-2-yl)pentanoate

HRID 1668538노트

반응식

HRID 1668538 반응식
ClCCl.[OH:4][CH2:5][C:6]1[N:11]=[C:10]([CH2:12][CH2:13][CH2:14][CH2:15][C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[CH:9]=[CH:8][CH:7]=1.C(N(C(C)C)CC)(C)C.[CH3:32][S:33](Cl)(=[O:35])=[O:34]>O>[CH3:32][S:33]([O:4][CH2:5][C:6]1[N:11]=[C:10]([CH2:12][CH2:13][CH2:14][CH2:15][C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[CH:9]=[CH:8][CH:7]=1)(=[O:35])=[O:34]

참가 물질

6

반응물 4

HCID 6344DichloromethaneHCID 31297Methanesulfonyl chlorideHCID 81531DiisopropylethylamineHCID 58105232t-Butyl 5-(6-hydroxymethylpyridin-2-yl)pentanoate

생성물 1

HCID 58105230t-Butyl 5-(6-methane-sulfonyloxymethylpyridin-2-yl)pentanoate

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a 200 mL round-bottom flask, 50 mL of dichloromethane, 2.78 g of t-butyl 5-(6-hydroxymethylpyridin-2-yl)pentanoate and 2.0 g of diisopropylethylamine were added, and the mixture was stirred at ice temperature for 10 minutes. To the reaction mixture, 0.89 mL of methanesulfonyl chloride was added dropwise, and the mixture was stirred at room temperature for 3 hours. Water was added to the reaction mixture, and the mixture was partitioned. The organic layer was washed with saturated aqueous sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, and then the solvent was removed. The residue was purified by chromatography on silica gel (n-hexane-ethyl acetate=3:1) to give 2.28 g of t-butyl 5-(6-methane-sulfonyloxymethylpyridin-2-yl)pentanoate as a yellow oil.

후처리

  1. stirringthe mixture was stirred at room temperature for 3 hours
  2. customthe mixture was partitioned
  3. washThe organic layer was washed with saturated aqueous sodium bicarbonate and brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customthe solvent was removed
  6. customThe residue was purified by chromatography on silica gel (n-hexane-ethyl acetate=3:1)

출처 및 근거

ORD 기록
ord-2baea6e96b8544059ce63e17b1a5ff9a
출처 데이터셋
uspto-grants-2011_08
특허 번호
US07989446B2

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