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Methyl Bromide → HCID 16720334、化合物

HRID 2240610
ノート
印刷プレビュー

反応式

HRID 2240610 の反応式
C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[CH3:11][O:12][C:13](=[O:23])[CH2:14][CH2:15][C:16]1[C:17](=[O:22])[NH:18][CH2:19][CH2:20][CH:21]=1.[CH3:24]Br>C1COCC1>[CH3:11][O:12][C:13](=[O:23])[CH2:14][CH2:15][C:16]1[C:17](=[O:22])[N:18]([CH3:24])[CH2:19][CH2:20][CH:21]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6323Methyl BromideHCID 2724254Sodium bis(trimethylsilyl)amideHCID 167203353-(2-Oxo-1,2,5,6-tetrahydro-pyridin-3-yl)-propionic acid methyl ester

生成物 1

HCID 16720334HCID 16720334、化合物収率 72%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

0.22 ml of 1.0M NaHMDS solution in THF (0.22 mM) was added to 0.5 ml of THF solution containing 80 mg 3-(2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl)-propionic acid methyl ester (f) prepared from the step 1 in Example 3 (0.44 mM) in a dropwise manner at −79° C. and then stirred for 30 min. After 0.48 ml of methyl bromide (0.48 mM) was added to the reaction mixture, the solution was stirred at 0° C. for 3 hrs. The reaction mixture was quenched by 2 ml of sat. NH4Cl solution and then the organic layer was extracted with ethyl acetate (7 ml). The combined organic layer was washed with 2 ml of sat. NH4Cl solution (2 ml) and 2 ml of sat. NaCl solution subsequently. Then the organic layer was dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resulting compound was purified by column chromatography on Silica gel with EtOAc solvent as an eluant to give 62 mg of the title compound (i2) (yield: 72%).

後処理

  1. stirringthe solution was stirred at 0° C. for 3 hrs
  2. customThe reaction mixture was quenched by 2 ml of sat. NH4Cl solution
  3. extractionthe organic layer was extracted with ethyl acetate (7 ml)
  4. washThe combined organic layer was washed with 2 ml of sat. NH4Cl solution (2 ml) and 2 ml of sat. NaCl solution subsequently
  5. dry with materialThen the organic layer was dried over anhydrous MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe resulting compound was purified by column chromatography on Silica gel with EtOAc solvent as an eluant

出典と根拠

ORDレコード
ord-2f43fe299bf74b58aff46e74b19ddff9
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07723376B2

反応ノート

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