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Triethylamine → methyl N-[(3-methyl-4'-nitrobiphenyl-4-yl)carbonyl]-L-valinate

HRID 2356827
ノート
印刷プレビュー

反応式

HRID 2356827 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=2)[CH:5]=[CH:6][C:7]=1[C:8]([OH:10])=O.C(Cl)(=O)C(Cl)=O.Cl.[CH3:27][O:28][C:29](=[O:35])[C@H:30]([CH:32]([CH3:34])[CH3:33])[NH2:31].C(N(CC)CC)C>C(Cl)Cl.CN(C=O)C>[CH3:1][C:2]1[CH:3]=[C:4]([C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=2)[CH:5]=[CH:6][C:7]=1[C:8]([NH:31][C@H:30]([C:29]([O:28][CH3:27])=[O:35])[CH:32]([CH3:34])[CH3:33])=[O:10]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 111190Methyl valinate hydrochlorideHCID 593852883-Methyl-4'-nitrobiphenyl-4-carboxylic acid

生成物 1

HCID 59385206methyl N-[(3-methyl-4'-nitrobiphenyl-4-yl)carbonyl]-L-valinate

試薬・触媒・溶媒 2

HCID 6228
Dimethylformamide
触媒
HCID 6344Dichloromethane溶媒2 回

反応条件

温度
50 °C

実験手順

3-Methyl-4′-nitrobiphenyl-4-carboxylic acid (0.50 g, 1.0 mmol) was dissolved in methylene chloride (10 mL), and then oxalyl chloride (0.25 mL, 0.29 mmol) was added, followed by one drop of DMF. The resulting mixture was stirred at 50° C. for 45 min and then concentrated under reduced pressure. The residue was dissolved in methylene chloride (5 mL) and added dropwise to an ice-cold mixture of L-valine methyl ester hydrochloride (0.39 g, 2.3 mmol), methylene chloride (10 mL), and triethylamine (1.08 mL, 7.75 mmol). The resulting solution was stirred at rt for 18 h. The mixture was concentrated under reduced pressure, and the residue was purified by column chromatography (50% EtOAc in hexanes). This yielded 0.653 g (91%) of the title compound. LC/MS m/z 370.9 (MH+), retention time 3.29 min. 1H NMR (400 MHz, CD2Cl2) δ 1.06 (dd, 6H), 2.32-2.39 (m, 1H), 2.55 (s, 3H), 3.78 (s, 3H), 4.71-4.78 (m, 1H), 6.33 (d, 1H), 7.42-7.52 (m, 3H), 7.82 (d, 2H), 8.26 (d, 2H).

後処理

  1. concentrationconcentrated under reduced pressure
  2. dissolutionThe residue was dissolved in methylene chloride (5 mL)
  3. stirringThe resulting solution was stirred at rt for 18 h
  4. concentrationThe mixture was concentrated under reduced pressure
  5. customthe residue was purified by column chromatography (50% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-8049b03c4d65493cb15ed82af97fb676
出典データセット
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07759376B2

反応ノート

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