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Triethylamine → Methyl 2-methanesulfonamido-3-methylbutanoate

HRID 1061677
ノート
印刷プレビュー

反応式

HRID 1061677 の反応式
C(N(CC)CC)C.Cl.[CH3:9][O:10][C:11](=[O:17])[CH:12]([CH:14]([CH3:16])[CH3:15])[NH2:13].[CH3:18][S:19](Cl)(=[O:21])=[O:20].C(OCC)(=O)C>C(Cl)Cl>[CH3:18][S:19]([NH:13][CH:12]([CH:14]([CH3:16])[CH3:15])[C:11]([O:10][CH3:9])=[O:17])(=[O:21])=[O:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 31297Methanesulfonyl chlorideHCID 12498813Valine, methyl ester, hydrochloride (1:1)

生成物 1

HCID 23199094Methyl 2-methanesulfonamido-3-methylbutanoate

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Triethylamine (6.7 ml) is added to a solution of DL-valine methyl ester hydrochloride (3.35 g, Reference compound No. 45-1) in methylene chloride (70 ml). The mixture is cooled with ice, methanesulfonyl chloride (1.9 ml) is added to the mixture, and the whole is stirred overnight. Ethyl acetate is added to the reaction mixture, the whole is washed with 0.1 N hydrochloric acid and saturated brine successively, and the organic layer is dried over anhydrous magnesium sulfate. The organic layer is concentrated under reduced pressure, and the resulting residue is purified by silica gel column chromatography to give the titled reference compound (4.00 g).

後処理

  1. additionis added to the mixture
  2. washthe whole is washed with 0.1 N hydrochloric acid and saturated brine successively
  3. dry with materialthe organic layer is dried over anhydrous magnesium sulfate
  4. concentrationThe organic layer is concentrated under reduced pressure
  5. customthe resulting residue is purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-9cae214f13154121bfbffdbfa25f4029
出典データセット
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06960575B2

反応ノート

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