Lithium Hydroxide → (2S)-3-Methyl-2-({[methyl(pent-4-en-1-yl)amino]carbonyl}amino)butanoic acid

HRID 1360107ノート

反応式

HRID 1360107 の反応式
[CH3:1][CH:2]([CH3:18])[C@H:3]([NH:8][C:9]([N:11]([CH3:17])[CH2:12][CH2:13][CH2:14][CH:15]=[CH2:16])=[O:10])[C:4]([O:6]C)=[O:5].[Li+].[OH-]>C1COCC1>[CH3:1][CH:2]([CH3:18])[C@H:3]([NH:8][C:9]([N:11]([CH3:17])[CH2:12][CH2:13][CH2:14][CH:15]=[CH2:16])=[O:10])[C:4]([OH:6])=[O:5]

参加物

4

反応物 2

HCID 3939Lithium HydroxideHCID 57617072Methyl (2S)-3-methyl-2-({[methyl(pent-4-en-1-yl)amino]carbonyl}amino)butanoate

生成物 1

HCID 57617111(2S)-3-Methyl-2-({[methyl(pent-4-en-1-yl)amino]carbonyl}amino)butanoic acid収率 95%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A 250 mL round bottom flask under nitrogen was charged with methyl (2S)-3-methyl-2-({[methyl(pent-4-en-1-yl)amino]carbonyl}amino)butanoate from the previous step, THF (40 mL), and aqueous LiOH (1 M, 60 mmol, 60 mL). The reaction mixture was stirred 18 hours. THF was removed by evaporation. The remaining aqueous mixture was poured into water and washed once with EtOAc. The aqueous layer was acidified with 1 M hydrochloric acid and extracted with EtOAc (3×). Combined organic extracts were dried with anhydrous NaSO4, filtered and evaporated to give the title compound as a pale oil (2.34 g, 9.66 mmol, 95%). LRMS m/e [M+H]+ 243.

後処理

  1. customTHF was removed by evaporation
  2. additionThe remaining aqueous mixture was poured into water
  3. washwashed once with EtOAc
  4. extractionextracted with EtOAc (3×)
  5. dry with materialCombined organic extracts were dried with anhydrous NaSO4
  6. filtrationfiltered
  7. customevaporated

出典と根拠

ORDレコード
ord-6f875324f5ce4552b958e58cd1965207
出典データセット
uspto-grants-2011_02
特許番号
US07879797B2

反応ノート

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